Part 607. PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES

• SUBPART A [§ 607.1 - § 607.7] - Subpart A—General Provisions
• SUBPART B [§ 607.20 - § 607.39] - Subpart B—Procedures for Domestic Blood Product Establishments
• SUBPART C [§ 607.40 - § 607.40] - Subpart C—Procedures for Foreign Blood Product Establishments
• SUBPART D [§ 607.65 - § 607.65] - Subpart D—Exemptions
• SUBPART E [§ 607.80 - § 607.80] - Subpart E—Establishment Registration and Product Listing Of Licensed Devices