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Code of Federal Regulations
Title 21
Chapter I
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
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A
General Provisions
B
Procedures for Domestic Blood Product Establishments
C
Procedures for Foreign Blood Product Establishments
D
Exemptions
E
Establishment Registration and Product Listing Of Licensed Devices