Reversed and remanded by published opinion. Judge NIEMEYER wrote the opinion, in which Judge SHEDD and Judge AGEE joined.
OPINION
The question presented by this appeal is whether a “biological opinion” issued by the National Marine Fisheries Service to the Environmental Protection Agency (EPA) pursuant to the Fisheries Service’s consulting role under the Endangered Species Act is subject to judicial review in the district court under the Administrative Procedure Act (APA), 5 U.S.C. § 704. The Fisheries Service, which provided the biological opinion to the EPA as part of the EPA’s process of reregistering for sale and use the insecticides ehlorpyrifos, diazinon, and malathion, concluded that the insecticides will destroy or harm Pacific salmonids and their habitat.
Pesticide manufacturers who hold the registrations for those insecticides commenced this action to challenge the biological opinion. The district court dismissed the action, concluding that the biological opinion is not reviewable under the APA because the EPA has not yet acted on the biological opinion and when it does issue a final order on whether to reregister the insecticides, the order, including the biological opinion, will be subject to judicial review in a court of appeals, as authorized in the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), 7 U.S.C. § 136n.
In this appeal from the district court’s dismissal order, we conclude that, under
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Bennett v. Spear,
I
The issue whether the Fisheries Service’s biological opinion is reviewable in court under § 704 of the APA or is only reviewable in a court of appeals after the EPA issues an order on the reregistration of the three insecticides at issue, as authorized by FIFRA, 7 U.S.C. § 136n, can better be resolved with an understanding of the interaction of two statutory schemes — the Endangered Species Act of 1973(ESA) and FIFRA. If FIFRA provides adequate judicial review of a biological opinion issued by the Fisheries Service to the EPA, then judicial review under the APA is unavailable. See 5 U.S.C. § 704 (authorizing judicial review if there is “no other adequate remedy in a court”).
A
Congress enacted the ESA “to conserve endangered species and threatened species,” 16 U.S.C. § 1531(c)(1), and to that end the ESA requires each federal agency in carrying out its functions to “insure” that its actions are “not likely to jeopardize the continued existence of any endangered species or threatened species or result in the destruction or adverse modification of habitat” deemed critical to such species, id. § 1536(a)(2). The Act requires that the Secretary of the Interi- or publish a list of those species that the Secretary determines to be endangered or threatened. Id. § 1533(c)(1). The Act also makes it unlawful for any person to “take” any endangered species, meaning to “harass, harm, pursue, hunt, shoot, wound, kill, trap, capture, or collect” the species. Id. § 1538(a)(1)(B); id. § 1532(19).
When a federal agency’s action is likely to jeopardize the existence of any endangered species, the agency is required to consult or confer with the Secretary of the Interior to engage in a process under which the Secretary provides an opinion evaluating the agency’s actions under the ESA. Id. § 1536(a). Consultation and conferral with the Secretary require that the agency, called the “acting agency,” interact with either the National Marine Fisheries Service or the U.S. Pish and Wildlife Service as “the consulting agency,” depending on the species or habitat involved. 50 C.F.R. §§ 402.01, 402.14. The consulting agency is then required to review all relevant information, to make evaluations of the acting agency’s proposed actions and the effects of its actions on the species or its habitat, and to issue a “biological opinion” (“BiOp”) as to whether the agency’s proposed action “is likely to jeopardize the continued existence of listed species or result in the destruction or adverse modification of critical habitat.” 50 C.F.R. § 402.14(g)(4), (h). The consulting agency’s issuance of a BiOp terminates the formal consultation between the acting agency and the consulting agency. 50 C.F.R. § 402.14(1).
The acting agency may then take under advisement the consulting agency’s recommendations, as stated in the BiOp, and decide how to proceed. If the acting.agency chooses to comply with the terms and conditions of the BiOp, the acting agency and its employees become exempt from
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prosecution for any violation of the ESA, thus providing a “safe harbor.” 16 U.S.C. § 1536(o)(2). The safe harbor also protects applicants for registration of pesticides or holders of those registrations. The acting agency may also choose not to comply with the BiOp. But in any event, the acting agency is not free to alter either the BiOp, which is the final decision of another agency, or the safe harbor created by the BiOp.
See Bennett,
B
The acting agency in this case is the EPA in its capacity as the Administrator of FIFRA.
FIFRA provides that “no person in any State may distribute or sell to any person any pesticide that is not registered [with the EPA] under this subchapter.” 7 U.S.C. § 136a(a). The EPA is required to register a pesticide if it determines that
(A) [the pesticide’s] composition is such as to warrant the proposed claims for it;
(B) its labeling and other material required to be submitted comply with the requirements of this subchapter;
(C) it will perform its intended function without unreasonable adverse effects on the environment; and
(D) when used in accordance with widespread and commonly recognized practice it will not generally cause unreasonable adverse effects on the environment.
Id. § 136a(c)(5). And FIFRA prohibits manufacturers from selling or distributing a registered pesticide in a manner inconsistent with the registration. Id. § 136j.
To ensure that registrations are up to date, 1988 amendments to FIFRA require the EPA to reregister any pesticide that was first registered before November 1, 1984. 7 U.S.C. § 136a-l(a). In the reregistration process, the EPA examines data to determine whether registered pesticides still meet FIFRA’s requirements, including the requirements that the pesticide perform without “unreasonable adverse effects” on the environment. If a registrant fails to conform to the reregistration process or no longer meets the requisite criteria, the EPA may deny reregistration and cancel the registration. Id. §§ 136a-l, 136d. Thus, whenever the EPA determines that a pesticide or its labeling does not comply with the provisions of FIFRA or “when used in accordance with widespread and commonly recognized practice, [the pesticide] generally causes unreasonable adverse effects on the environment,” the EPA can cancel the pesticide’s registration. Id. § 136d(b).
FIFRA provides for judicial review of the EPA’s pesticide registration decisions. 7 U.S.C. § 136n. If the EPA issues an order following a public hearing, its order is reviewable exclusively in the courts of appeals. If, however, the EPA has not issued an order following a hearing, its inaction is reviewable in the United States district courts. Id.
II
Chlorpyrifos was first registered in 1965; diazinon, in 1956; and malathion, in 1956. Accordingly, under FIFRA’s 1988 amendments requiring the reregistration of pesticides registered before November 1, 1984, these insecticides became subject to reregistration by the EPA.
In January 2001, several environmental groups filed a suit against the EPA in the Western District of Washington, alleging that the EPA was violating the ESA by failing to consult with the Secretary of the Interior with respect to the EPA’s reregistration and continuing approval of 54 ac
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tive ingredients in pesticides, including the three insecticides involved in this case. The district court agreed with the plaintiffs and ordered the EPA to initiate consultation with the National Marine Fisheries Service in connection with the pesticide ingredients.
Wash. Toxics Coalition v. EPA,
Civ. No. 01-132,
When the Fisheries Service failed for several years to issue its BiOps pursuant to the EPA’s formal consultation, an environmental group filed suit in the Western District of Washington to require the Fisheries Service to issue its BiOps, as required by the ESA. See Northwest Coalition for Alternatives to Pesticides v. Nat’l Marine Fisheries Serv., Civ. No. 07-1791 (W.D.Wash. filed Nov. 5, 2007). The Fisheries Service settled the suit on July 30, 2008, by agreeing to issue its first BiOp within 90 days. One day after the settlement agreement, the Fisheries Service issued a draft of its first BiOp, which addressed the effects of chlorpyrifos, diazinon, and malathion. The draft concluded that these insecticides would jeopardize critical habitat and prey for “evolutionarily significant units” of 28 Pacific salmonid species that are listed as endangered or threatened. Shortly after issuing the draft BiOp, the Fisheries Service opened an online docket to enable persons to comment on the draft until September 15, 2008. On November 18, 2008, it issued its final BiOp on the three insecticides.
The final BiOp concluded that chlorpyrifos, diazinon, and malathion would jeopardize numerous salmonid species and adversely affect critical habitat for them. Specifically, it found that the exposure to these pesticides will kill salmonids and, even at low exposure levels, will reduce salmonid growth, reduce the availability of prey, and impair salmonids’ swimming and olfactory senses. In short, the Fisheries Service’s BiOp concluded that reregistration of the insecticides would jeopardize the survival of 27 of 28 listed salmonid species and adversely affect the critical habitat of 25 of the 26 species for which critical habitat had been designated. The BiOp, however, recommended a “reasonable and prudent alternative” to the current registrations by (1) requiring setbacks for the application of insecticides that would be 500 feet away from salmonid habitats for ground applications and 1,000 feet for aerial application; (2) limiting application in high wind; (3) requiring a 20-foot strip of vegetation near surface waters connected to salmonid habitats; (4) requiring regular reports concerning fish mortality; and (5) limiting application when soil moisture is, or is likely to become, high. The BiOp also issued an “Incidental Take Statement” requiring that the EPA implement a Fisheries Service approved effectiveness monitoring plan.
Upon the Fisheries Service’s issuance of the final BiOp, the formal consultation between the EPA and the Fisheries Service ended. See 50 C.F.R. § 402.14(1).
The EPA has yet to release its decision on the reregistration of chlorpyrifos, diazinon, and malathion. But it has advised the Fisheries Service by letter that it intends to implement only some of the Fisheries Service’s proposed label changes and to adopt its own buffer requirements, which the EPA stated would accomplish the Fisheries Service’s goals. See Letter from Richard P. Keigwin, Jr., Director, Special Review and Reregistration Division, U.S. EPA, to James H. Lecky, Director, Office of Protected Resources, *264 Nat’l Marine Fisheries Service (Sept. 10, 2009), available at http://www.epa.gov/ oppfeadl/endanger/litstatus/wtc/.
Dow AgroSciences LLC, Makhteshim Agan of North America, Inc., and Cheminova, Inc. USA, manufacturers of pesticides and holders of registrations for chlorpyrifos, diazinon, and malathion (collectively, “Pesticide Manufacturers”), commenced this action in the district court against the National Marine Fisheries Service under § 704 of the APA to obtain judicial review of the Fisheries Service’s final BiOp governing chlorpyrifos, diazinon, and malathion. In their complaint, the Pesticide Manufacturers allege that the Fisheries Service did not comply with the ESA’s mandate that its BiOp be based on the “best scientific and commercial data available,” 16 U.S.C. § 1536(a)(2). They allege that the Fisheries Service ignored superior scientific studies submitted by them and supported by the EPA. Additionally, they allege that the Fisheries Service accelerated the timeline for issuing the final BiOp, causing the agency not to address material comments submitted in response to the draft BiOp.
On the motion of the Fisheries Service, the district court dismissed the action for lack of jurisdiction.
Dow AgroSciences LLC v. National Marine Fisheries Service,
In the case before this Court the Biological Opinion was prepared during an EPA licensing proceeding under FI-FRA. If the EPA relies on the Biological Opinion and seeks to cancel Plaintiffs’ pesticide registrations, EPA will have to issue an order under FIFRA. Any such order could only be challenged in a federal court of appeals.
As the federal courts of appeals have exclusive jurisdiction over FIFRA orders, the Court finds that it does not have jurisdiction over matters that could directly affect the exclusive jurisdiction.
Id. at 513. From the entry of that July 29, 2009 order, the Pesticide Manufacturers timely filed this appeal.
Ill
The Pesticide Manufacturers contend that the Fisheries Service’s BiOp was a final agency action, as the term is used in the APA, that is subject to judicial review in the district court.
See
5 U.S.C. § 704. They argue that the BiOp was the “consummation of the [Fisheries Service’s] decisionmaking process” and has “direct and appreciable legal consequences,”
Bennett v. Spear,
The National Marines Fisheries Service contends that even if the BiOp is a final agency action, it would be reviewable in a district court under the APA only if there were “no other adequate remedy in a court.” 5 U.S.C. § 704. The Fisheries Service claims that in this case “there will be adequate review of the BiOp by the court of appeals on review of any decision by the EPA to cancel or alter the registrations as provided by FIFRA’s special statutory jurisdictional provision,” 7 U.S.C. § 136n. It maintains, accordingly, that judicial review now in the district court is not authorized by the APA.
Section 704 of the APA provides that “final agency action for which there is no other adequate remedy in a court [is] subject to judicial review.” 5 U.S.C. § 704 (emphasis added). Thus we must determine (1) whether a BiOp is a final agency action, and (2) whether there is another adequate remedy in a court for review of the BiOp.
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On the first question, the Supreme Court has held that a BiOp is a final agency action. First, it “mark[s] the ‘consummation’ of the agency’s decisionmaking process” — the Fisheries Service’s work as a consulting, specialist agency.
Bennett,
[The action agency] runs a substantial risk if its (inexpert) reasons turn out to be wrong. A Biological Opinion of the sort rendered here alters the legal regime to which the action agency is subject____ [T]he Biological Opinion’s Incidental Take Statement constitutes a permit authorizing the action agency to “take” the endangered or threatened species so long as it respects the Service’s “terms and conditions.” The action agency is technically free to disregard the Biological Opinion and proceed with its proposed action, but it does so at its own peril (and that of its employees) for “any person” who knowingly “takes” an endangered or threatened species is subject to substantial civil and criminal penalties, including imprisonment.
On the second question, whether there is another adequate remedy in a court for review of the BiOp, FIFRA does provide for judicial review in the court of appeals of “any order issued by the Administrator [the EPA] following a public hearing.” 7 U.S.C. § 136n(b) (emphasis added). But because a BiOp is not an “order issued by the Administrator [the EPA],” the plain language does not provide statutory support for an argument that a BiOp issued by the Fisheries Service can be subject to judicial review as part of the FIFRA Administrator’s decision.
Nonetheless, an exclusive judicial review provision applies to “all issues inhering in the controversy.”
City of Tacoma v. Taxpayers of Tacoma,
First,
the BiOp has immediate and independent legal consequences that cannot be changed on later review of the EPA’s action on reregistration, even if the EPA relies on the BiOp. The EPA’s reregistration of pesticides involves a broad array of different issues relating to whether the pesticides perform as claimed, their labeling, and their effect on the environment.
See
7 U.S.C. § 136a(c)(5). Even though the EPA must also consider a BiOp, it cannot change it or modify it.
See Bennett,
In this case, the Fisheries Service concluded that the use of chlorpyrifos, diazinon, and malathion “is likely to jeopardize the continued existence” of Pacific salmon-ids and “is likely to destroy or adversely modify” their habitats. The Fisheries Service conditioned any further use of chlorpyrifos, diazinon, and malathion on modifications in their use that were significant. The conditions require that the insecticides not be applied in specified areas near salmonid habitats and that they not be applied anywhere when certain weather factors exist. The conditions also require that any person applying the insecticides report “all incidents of fish mortality that occur within four days of application.”
Most importantly, the BiOp creates a safe harbor
for all persons. See
16 U.S.C. § 1536(o)(2). If a person, including a government employee, knowingly “takes” an endangered or threatened species, that person is subject to civil and criminal penalties. If, however, a person “takes” a protected species while complying with the BiOp’s terms, that person is insulated from liability. Thus, as the Supreme Court has noted, while a BiOp does not create a legally binding prohibition, “[i]n reality [the BiOp] has a powerful coercive effect.”
Bennett, 520
U.S. at 169,
In this way, therefore, any continued use of chlorpyrifos, diazinon, and malathion is subject to the Fisheries Service’s BiOp, which “alters the legal regime to which the action agency [and the Pesticide Manufacturers] is subject,”
Bennett, 520
U.S. at 169,
Second, if the EPA were to choose not to rely on the Fisheries Service’s BiOp, then the BiOp would not be subject to any review in a judicial proceeding challenging the FIFRA reregistration order. Yet, the BiOp would still exist, having significant legal consequences, as we have noted, because it makes final findings and defines the safe harbor from civil and criminal liability. Thus, after the EPA’s reregistration decision, the Pesticide Manufacturers would still be governed in part by the BiOp. If the Pesticide Manufacturers took an action that complied with the EPA’s reregistration decision, but did not comply with all of the terms of the BiOp, they would not be protected by the BiOp’s safe harbor. In such a situation, the Pesticide Manufacturers would still be subject to the legal consequences for “taking” a protected species as defined by the ESA. Only the BiOp protects persons from liability.
Third,
when a court of appeals reviews the EPA’s
reliance on a BiOp
issued by the Fisheries Service, the court’s review would not be the same as if the district court were to review the BiOp itself directly under the APA. When a court of appeals reviews
the EPA’s reliance
on a BiOp, it would determine only whether the EPA’s reliance was arbitrary and capri
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cious. But only by direct judicial review by the district court under the APA could the BiOp’s findings and conclusions themselves be challenged.
See City of Tacoma v. FERC,
Fourth,
if the EPA were to choose to follow the Fisheries Service’s BiOp, any challenge to the EPA’s reliance on the BiOp on judicial review could not itself cause the EPA to alter the BiOp. The EPA does not have that authority, and the Fisheries Service would not be a party to the proceeding. The only issue that could be reviewed would be the reasonableness of
the EPA’s reliance
on the BiOp. Even if a court were to find that the EPA’s reliance was arbitrary and capricious because of an unreasonable or unsupportable BiOp, the remedy would relate only to reregistration; the BiOp’s final findings and definition of the safe harbor would continue to be in effect as final agency action,
see
50 C.F.R. § 402.14(1), and its legal consequences could still not be altered, regardless of the EPA’s reregistration order.
See Bennett,
Fifth,
the plain language of FIFRA’s judicial review provisions does not contain “clear and convincing evidence” that Congress intended FIFRA’s judicial review provisions to govern review of a BiOp issued by a different agency — the Fisheries Service, which is within the Department of Commerce.
See Abbott Labs. v. Gardner,
In sum, the BiOp in this case was the final agency action of the Fisheries Service, which has ongoing legal consequences, and it could not be altered, modified, or changed by the EPA during its registration process under FIFRA. In some circumstances, the BiOp might not even be considered by the EPA, leaving review under the APA as the only avenue for judicial review. And if the EPA followed the BiOp, only the EPA’s action in relying on the BiOp, not the adequacy of the BiOp itself, could be reviewed. In these circumstances, a challenge to an EPA order on registration does not pro *268 vide an adequate judicial review of the BiOp.
The circumstances of this case and the statutory roles of the agencies involved distinguish this case from those in which agency actions have been found to inhere in final agency actions. For example, in
Telecommunications Research & Action Ctr. v. FCC,
The Fisheries Service relies on
City of Tacoma v. FERC,
The procedural posture in this case is different from that in
City of Tacoma,
where reliance on the BiOp was challenged in connection with the acting agency’s final order. In the procedural posture presented here, where judicial review of a BiOp itself is sought prior to the acting agency’s final action, courts have allowed for judicial review of the BiOp, as we do here.
See Miccosukee Tribe v. United States,
For all of the foregoing reasons, we hold the district court had jurisdiction over the Pesticide Manufacturer’s complaint and it therefore, erred in dismissing this action for lack of jurisdiction.
IV
The National Marine Fisheries Service also contends that plaintiffs’ claims are not ripe for decision because resolution of them may prove unnecessary once the plaintiffs have exhausted their administrative remedies before the EPA under FI-FRA.
In resolving the Fisheries Service’s ripeness argument, we assess two factors: (1) the fitness of the issue for judicial decision
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and (2) the hardship to the parties of withholding court consideration.
Abbott Labs.,
The Fisheries Service’s argument here is based on its view that the BiOp could become insignificant. As it argues in its brief, the
EPA is not required to adopt the reasonable and prudent alternative provided in the BiOp, and EPA may decide to take actions that are acceptable to the Registrants by either declining to modify the FIFRA registrations or adopting less stringent restrictions — in which case the dispute may never materialize. Alternatively, if EPA decides to take a FIFRA action to which the registrants object, FIFRA provides the Registrants an opportunity to demand an administrative hearing. The result of the FI-FRA administrative hearing may satisfy the Registrants without the need for court intexrvention.
As we have noted, the Fisheries Service’s BiOp represents the culmination of its decisionmaking process. Under the agency’s regulations, the Fisheries Service’s role in consulting with the EPA “is terminated with the issuance of the biological opinion.” 50 C.F.R. § 402.14(0- Accordingly, there is no reason to conclude that the Fisheries Service would crystallize its policy at some later time.
See Reg’l Mgmt. Corp.,
Accordingly, we conclude that a challenge to the BiOp is ripe for judicial review at this time.
For the reasons given, we reverse the district court’s order dismissing this case and remand for further proceedings.
REVERSED AND REMANDED
