The primary question on this appeal is whether a defendant can be convicted of “defrauding” an agency of the United States under the general federal conspiracy statute, 18 U.S.C. § 371, if he did not contact agency personnel or submit docmnents to the agency. The question arises on an appeal by Pascal Ballistrea from the September 26, 1995, judgment of the District Court for the Western District of New York (Richard J. Arcara, Judge), convicting him, after a jury trial, of five counts arising under substantive provisions of the Food, Drug, and Cosmetics Act (“FDCA”), 21 U.S.C. § 301
et seq.,
two counts of conspiracy to defraud an agency of the United States, 18 U.S.C. § 371, and one count of making а
*830
false statement to the United States, 18 U.S.C. § 1001. We conclude that defendant was properly convicted of conspiracy to defraud the Food and Drug Administration (“FDA”) because he conspired with others to interfere with or obstruct the FDA’s lawful function of regulating the interstate distribution of medical devices and new drugs by deceit, trickery, and dishonest means. We also conclude that defendant’s numerous challenges relating to trial proceedings, jury charge, and sentencing are without merit. However, we vacate defendant’s conviction under 18 U.S.C. § 1001 because the element of materiality was not submitted to the jury as required by
United States v. Gaudin,
— U.S. -,
Background
In the late 1980s, Life Energy Rеsources, Ltd. (“LER”), a New York corporation, began conducting the business of ordering, storing, and distributing a variety of health-related devices and products through a multilevel marketing network. LER’s marketing plan provided that members of the general public could purchase its products only through an official LER distributor, or by becoming LER distributors themselves. Each potential distributor had to be sponsored by an existing distributor and was required to sign a distributorship agreement with LER stating that he or she would not make medical claims or use unofficial literature or marketing aids to promote LER products. Distributors profited both from the price differential between LER’s sale price to them and their sale price to customers, and from sales made by other distributors whom they had originally sponsored — in the amount of five percent of the “downstream” distributors’ gross sales.
Appellant Ballistrea and his partner Michael Ricotta were at the top of the LER distribution network. They formed a partnership under the name East Coast Marketing that sold LER products directly to end users and sponsored downstream distributors. Additionally, Ballistrea, who had years of experience in multi-level distribution schemes, helped to set up LER’s distribution system at the company’s founding. For his efforts, LER awarded him one percent of all gross commissionable sales.
Two products sold by LER were the REM SuperPro Frequency Generator (“REM”) and the Lifemax Miracle Cream (“Miracle Cream”). The REM, which sold for $1,350 to distributors, was a small box powered by electricity that ran currents through the feet and body of the user. It was officially described by LER as a “pulse generating instrument.” The Miracle Cream was described by LER as an “excellent moisturizer and skin softener,” but “possibly much more.” Like all LER products, the REM and the Miracle Cream came with a disclaimer stating that they were not to be used for the “cure, treatment, mitigation, prevention, or diagnosis of diseases.” These products were sold by LER until July 1990, when their sales and distribution were transferred to a newly formed corporation named New Millennium. New Millennium used the same multi-level marketing format as LER, and Ballistrea and Ricotta became distributors for this company upon its establishment.
The evidence showed that Ballistrea and Ricotta distributed literature and audiotapes to many potential downstream distributors and customers — some of whom were undercover Government agents — touting the REM and the Miracle Cream as having medicinal effects. Some materials, for instance, claimed that pulse stimulation devices such as the REM could cure cancer, staph infections, and other serious diseasеs. Other literature claimed that the Miracle Cream could alleviate the discomforts of premenstrual syndrome and reverse the effects of osteoporosis. Both Ballistrea and Ricotta also personally told many potential purchasers, including several who were gravely ill or had sick relatives and friends, about the alleged curative powers of these products.
Ballistrea and his partner knew that the REM and the Miracle Cream were not FDA approved and sought to conceal their activities from the Government. Their knowledge of the inappropriateness of their acts is demonstrated both by thе distributorship agreement explicitly forbidding LER distributors *831 from making medical claims concerning LER products and by a LER newsletter notifying all distributors to stop using unofficial literature to tout the curative powers of LER products. Additionally, both Ballistrea and Ricotta told undercover Government agents, posing as potential downstream distributors, that they should use the unofficial literature to market the products, especially to customers who were ill, but should take great care to ensure that their use of this information is not discovered by the FDA. Ballistrea stated on a training video for LER phone operators that they should be careful about touting LER prоducts as medical aids, to callers because “it could be the FDA calling.” Ballistrea also informed an undercover postal inspector that he helped to set up New Millennium to distribute the REM and the Miracle Cream because of concerns that the FDA was acting against LER and its distributors for improperly distributing these products.
Ballistrea and Ricotta were tried separately. Ricotta was convicted of conspiring to defraud the FDA and of violating various provisions of the FDCA and sentenced to 41 months’ imprisonment. Ballistrea was convicted on two counts of conspiracy to defraud the FDA (one for the RÉM and one for the Mirаcle Cream), 18 U.S.C. § 371, five counts of introducing unapproved medical devices and new drugs into interstate commerce, 21 U.S.C. §§ 331(a) & 333(a)(1), and one count of making a false statement to federal officials, 18 U.S.C. § 1001. Ballistrea was also sentenced to 41 months’ imprisonment.
Discussion
I. Conspiring to Defraud the United States
Ballistrea contends that the Government failed to prove the conspiracy to defraud the FDA charges because there was no evidence of “actual or active contact” between him or Ricotta and the FDA or its agents. We reject this argument because the defraud prong of the federal conspiracy statute does not require such a showing оf actual contact.
The general federal conspiracy statute punishes a conspiracy that has either of two objects: “to commit any offense against the United States, or to defraud the United’ States, or any agency thereof in any manner or for any purpose.” 18 U.S.C. § 371. Ballistrea was charged under section 371 both with conspiracy to defraud the FDA, by interfering with its lawful function of regulating the interstate distribution of medical devices and drugs, and with conspiracy to violate specific sections of the FDCA prohibiting the introduction of unapproved medical devices and drugs into interstate commerce. Count I concerned the REM and charged a conspiracy with two objectives: to defraud the FDA and to violate substantive provisions of the FDCA. Count IX concerned the Miracle Cream and similarly charged a dual-object conspiracy. In each count, the conspiracy to defraud the FDA constituted a felony, though the conspiracy to violate substantive provisions of the FDCA constituted a misdemeanor because a violation of these substantive provisions constituted a misdemeanor. See id. The jurors specifically indicated on the verdict form that they found Ballistrea guilty on both aspects of the conspiracies charged in Counts I and IX.
A conspiracy to defraud under section 371 embraces “any conspiracy for the purpose of impairing, obstructing, or defeating the lawful function of any department of government.”
Dennis v. United States,
Ballistrea’s contention that the required element of “obstruction” or “interference” must involve actual contact between the defendant and the Government agency — for instance, through the making of misrepresentations to agency officials or the submitting of false information to the agency — finds no support in the ease law. In
Nersesian,
for instance, a defendant conspired with others to structure bank transactions so that no individual transaction involved more than $10,000.
The Government proved at trial that Bal-listrea and Ricotta — with knowledge that their marketing scheme was in contravention of the law — repeatedly instructed persons to whom they had sent unauthorized literature touting the medicinal powers of the REM and the Miracle Cream to conceal their use and possession of this information because the FDA might discover their unlawful activity. Moreover, Ballistrea helped to organize and became a distributor in a new company — New Millennium — formed to sell these products because the FDA began to investigate LER’s- distribution of the REM and the Miracle Cream. Although the creation of New Millennium ultimately failed to throw the FDA off Ballistrea’s scent, such evidence of active concealment and evasion is more than sufficient to establish that Ballistrea agreed with Ricotta and others to obstruct, through deceit, trickery, or dishonest means, the FDA’s lawful function of regulating the marketing and distribution of medical devices and drugs in the United States.
See United States v. Sturman,
The cases cited by Ballistreа to support his reading of the conspiracy statute are inappo-site, for they do not involve convictions under the “defrauding” prong of 18 U.S.C. § 371, but convictions under 21 U.S.C. § 333(a)(2), which governs violations of 21 U.S.C. § 331(a) (prohibiting the introduction of unapproved medical devices and drugs into intérstate commerce) committed with an “intent to defraud or mislead” either end users or Government agencies.
2
See, e.g., United States v. Arlen,
*834 II. Jury Charge Claims
Ballistrea. challenges several aspects of the jury instructions. With the exception of his argument directed toward the District Judge’s charge on the 18 U.S.C. § 1001 count, we find defendant’s contentions to be without merit.
1. 18 U.S.C. § 1001
Ballistrea contends that the District Judge erred by not providing a specific instruction to the jury on the element of materiality in the charge on Count VIII, which alleged that defendant made a false statement to FDA investigators. Because defendant did not object to this charge at trial, this Court’s review will be. for plain error.
United States v. Tillem,
Thе false statement at issue was made by defendant to Government investigators during the execution of a search warrant at defendant’s home that resulted in the seizure of literature and tapes touting the BEM and the Miracle Cream as having medicinal powers. Defendant declared in a signed statement that he had not distributed the seized materials for more than one year. At the time of the statement, Government officials had ample evidence that this statement was false. Defendant does not now contend that the statement was trae.
In his instructions to the jury on the section 1001 count, the District Judge first read the language of this provision, whiсh provides that whoever “knowingly and willfully falsifies, conceals or covers up by any trick, scheme or devise a material fact” shall be guilty of this offense. However, the District Judge did not identify materiality as an element and listed only the following four as “essential elements” of the section 1001 offense: that defendant (1) knowingly and willfully (2) made a statement, (3) which was false, and (4) which was within the jurisdiction of an agency of the United States. Indeed, during a post-trial hearing on this very issue, the Judge acknowledged that he “did not require the jury to find that the alleged false statement was material” because he had followed then-controlling Second Circuit law in this matter.
See United States v. Elkin,
In
United States v. Gaudin,
— U.S. -,
*835
Because defendant did not timely object to the section 1001 charge, this Court can reverse only for “plain error.” Fed. R.Crim.P. 52(b). In
United States v. Olano,
The first two
Olano
requirements are easily met. First, as a result of
Gaudin
and
All,
the jury charge was erroneous. Second, the error was plain because it is clear undеr “current law,” meaning the law existing at the time of the appeal.
United States v. Viola,
2. Jury Charge on Counts I and IX
Defendant сomplains that the District Judge’s charge on the two conspiracy founts was confusing and created the possibility that the jury, while finding the evidence sufficient to convict him only under the misdemeanor, prong of the two counts, mistakenly convicted him under the felony “defrauding” prong. Because defendant did not timely raise this objection, we review for plain error,
Tillem,
As discussed earlier, each of the section 371 counts charged a conspiracy with two objectives: a felony conspiracy to defraud the FDA and a misdemeanor conspiracy to violate a specific FDCA provision. Although defendant implies that this manner of charging, in and of itself, is improperly duplicitous, this Circuit has approved the use of such indictments.
See, e.g., United States v. Southland Corp.,
Our review of the record leads us to conclude that no possibility of prejudice resulted to defendant from the District Court’s charge on Counts I and IX.- Simply put, the District Judge, specifically and separately, discussed the elements of felony conspiracy to defraud and the elements of misdemeanor conspiracy to violate provisions of the FDCA. He also repeatedly distinguished the felony conspiracy aspect from the misdemeanor conspiracy aspect in both counts. Such explication adequately eliminates the risk of misunderstanding,
cf. Williams,
3. Responsible Party
Defendant contends that the District Judge erred in refusing his request to instruct the jury that a required element of all the FDCA-related offenses was that defendant was a “legally responsible party,’-’
ie:,
someone with sufficient authority to seek
*836
FDA approval or registration for the REM and the Miracle Cream. Tó prevail, defendant must show that his requested charge accurately stated the governing law and that the charge as given prejudiced him.
United States v. Dove,
Defendant erroneously reads
United States v. Park,
Park is irrelevant to the present ease, however, because the Government did not prosecute Ballistrea for failing to -prevent a viоlation of the FDCA by third parties under Ms authority. Rather, it prosecuted him for personally violating the FDCA by his own conduct of causing unapproved medical devices and drugs to be introduced into interstate commerce.
The relevant statutory provisions clearly cover defendant’s conduct:
The following acts and the causing thereof are prohibited:
(a) the introduction or delivery for introduction into interstate commerce of any food, drug, device, or cosmetic that is adulterated or misbranded.
21 U.S.C. § 331(a). The statute makes no distinction as to whether the person who has personally introduced or caused the introduction of an unapproved or unregistered product into cоmmerce is a “responsible party.” The penalty provision governing tMs section also makes no such distinction: “Any person who violates a provision of section 331 ... shall be imprisoned ... or fined_” As one court has put it, “it is unnecessary to go beyond the plain language of the statute. ‘Any’ means any.”
United States v. General Nutrition, Inc.,
Park held that parties charged with failing to prevent violations of the FDCA can be convicted only if they held positions of authority enabling them to rectify or prevent the violations; it did not impose a similar requirement of responsible party status when the defendant is charged with personally violating the FDCA by Ms own conduct of introducing, or causing the introduction of, unapproved devices and drugs into interstate commerce. The District Court’s refusal to accede to defendant’s charge request was not erroneous.
III. Defense Witness Immumty
Defendant contends that the District Court erred in denying his request to the Court to require the Government to
*837
grant immunity to two high-level LER officials whom defendant wished to call as witnesses. In
United States v. Turkish,
Nothing in the record indicates that the Government had granted immunity tо its witnesses, and refused to grant immunity to defendant’s witnesses, in order to gain a tactical advantage. Moreover, there is no indication that the testimony sought by defendant would have been exculpatory or even relevant. Defendant’s hope in seeking this testimony was to show that these witnesses, and not the defendant, were the parties responsible for seeking FDA approval and registration for the REM and the Miracle Cream. As noted previously, however, defendant was not charged with failing to prevent violations of the FDCA by third parties who neglected to register or seek FDA approval for these products, but with personally introducing or causing the introduction of these products into interstate commerce. The mere fact that these witnesses might also be liable for violations of the FDCA under Park is not relevant to the issue of defendant’s own guilt. The District Court properly declined to order the Government to grant immunity to defendant’s witnesses.
IV. Jury Deliberations
Defendant contends that improper oral communication occurred between the jury, the District Judge, and the prosecutor. The complaint concerns a request by the jury to hear certain tape recordings introduced into evidence and the attempt by the prosecutor and the District Judge to ascertain the precise extent of the jury’s request through oral colloquy.
Although the District Court did not fully comply with the procedures outlined in
United States v. Ronder,
V. Sentencing
Defendant makes a number of objections to his sentence, all of which are without merit. We discuss defendant’s objection to the two-level enhancement under U.S.S.G. § 3C1.1 for obstruction of justice, however, because the conduct giving rise to this enhancement—a false statement made to FDA investigators during the execution of a search warrant at defendant’s home—also underlies his conviction under 18 U.S.C. § 1001, which we vacate in this opinion. Although defendant’s materiality claim' is suсcessful in the section 1001 context, it does not bar a Guidelines enhancement.
Even if we assume that the definition of materiality is the same in both contexts, the question of whether the false statement is material for the purpose of the obstruction enhancement, unlike the seem *838 ingly similar question in the section 1001 context, is a question expressly for the sentencing judge, and not the jury, to decide. Therefore, although the failure to instruct the jury on materiality voids conviction on the section 1001 count, there is sufficient basis to support the Court’s finding of materiality and its imposition of an obstruction of justice enhancement.
Conclusion
We reject Ballistrea’s remaining contentions without discussion. For the foregoing reasons, defendant’s convictions for conspiracy to defraud the FDA and for violating substantive provisions of the FDCA are affirmed. His conviction under 18 U.S.C. § 1001 is vacated. We remand this ease to the District Court for entry of a revised judgment.
Notes
.
In Ratzlaf v. United States,
Although
Nersesian
suggests an interpretation of the antistructuring statute later repudiated by
Ratzlaf, see Nersesian,
. Prior to 1988, section 333(a)(2) was designated as section 333(b).
. One rеported decision does contain language supporting Ballistrea’s interpretation of section 371’s defrauding prong. In
United States v. Haga,
Noting that indictments under the defrauding prong "ordinarily described clear interference and active contact with governmental agency functions” and allege "more than completely external interference with the working of a governmental program or disregard for federal laws,” id. at 1040, the Fifth Circuit concluded that the defendant was indicted under the specific offense prong of section 371. Id. at 1043; see id. at 1041 ("[F]or a section 371 ‘conspiracy to defraud’ conviction to stand, the essence of the conspiracy must at least involve a showing of more than inadvertent contact with a governmentаl agency or incidental infringement of government regulations. ...”). Because the variance between the offense of indictment and the offense of conviction was not harmless, the defendant’s conviction was vacated.
Because the language from Haga is found in a factual and legal context significantly different from that of the present case, it is difficult to speculate whether the Court in Haga would have found that Ballistrea’s active concealment of his illicit activities from FDA regulators constituted mere “external interference with governmental agency functions” or "inadvertent contact with a governmental agency."
. Our recent decision in
United States v. Klausner,
Klausner
recоgnized, however, that where it is necessary to make factual determinations as to what statement was made by the defendant and what decision the agency was trying to make, the question of materiality must be submitted to the jury.
Id.
Indeed, the Court explicitly noted that although the issue of materiality in many statutes is a question of law for the judge, the " 'exception has been section 1001 cases, in which we have held that it is an element of the crime that must be determined by the jury.’ ”
Id.
at 60 (quoting
United States v. Taylor,
. In the section 1001 context, a false statement is “material” if it has the natural tendency to influence or be capable of affecting the Government's action.
See, e.g., Klausner,
