1. Collections
  2. Code of Federal Regulations
  3. Title 21
  4. Chapter I
  5. Subchapter F

Part 607

21 C.F.R. Part 607

Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices

AGeneral ProvisionsBProcedures for Domestic Blood Product EstablishmentsCProcedures for Foreign Blood Product EstablishmentsDExemptionsEEstablishment Registration and Product Listing Of Licensed Devices
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