{"data":{"id":"us/21-cfr-607.35","jurisdiction":"us","citation":"21 CFR 607.35","heading":"Blood product establishment registration number.","body":"An establishment registration number will be assigned to each blood product establishment registered in accordance with this part.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER F—BIOLOGICS","PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES","Subpart B—Procedures for Domestic Blood Product Establishments"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"5d26f0ef03706fd172c7eb3b313f7a2d403af8bad1336ad8d455f8cd1cf35c1a","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-607.31","next":"us/21-cfr-607.37"},"notice":"GroundRules: Original legal text. Not legal advice."}