21 CFR 607.7
§ 607.7 Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products.
United States · 21 CFR — Food and Drugs · Status: effective
Cite this
- Citation
- 21 CFR 607.7, § 607.7 Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/88391
- Permanent ID
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Full text
All owners or operators of establishments that engage in the manufacturing of blood products are required to register, pursuant to section 510 of the Federal Food, Drug, and Cosmetic Act. Registration and listing of blood products must comply with this part. Registration does not permit any blood bank or similar establishment to ship blood products in interstate commerce.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.