Part 607 - ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
- Subpart A - GENERAL PROVISIONS (§§ 607.1 — 607.7)
- Subpart B - PROCEDURES FOR DOMESTIC BLOOD PRODUCT ESTABLISHMENTS (§§ 607.20 — 607.39)
- Subpart C - PROCEDURES FOR FOREIGN BLOOD PRODUCT ESTABLISHMENTS (§ 607.40)
- Subpart D - EXEMPTIONS (§ 607.65)
- Subpart E - ESTABLISHMENT REGISTRATION AND PRODUCT LISTING OF LICENSED DEVICES (§ 607.80)