Federal (United States) · Regulations
Part 607 — ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
16 sections
5 groups
- Subpart A — General Provisions3 sections
- Subpart B — Procedures for Domestic Blood Product Establishments10 sections
- Subpart C — Procedures for Foreign Blood Product Establishments1 section
- Subpart D — Exemptions1 section
- Subpart E — Establishment Registration and Product Listing Of Licensed Devices1 section