{"data":{"id":"us/21-cfr-213.1","jurisdiction":"us","citation":"21 CFR 213.1","heading":"Scope.","body":"The regulations in this part contain the minimum current good manufacturing practice for preparation of medical gases for administration to humans or animals.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 213—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICAL GASES","Subpart A—General Provisions"],"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":"94b117cc89709c358a99f18cd01dccf7e5ba7db03bec716564056f317741f2a7","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-212.110","next":"us/21-cfr-213.3"},"notice":"GroundRules: Original legal text. Not legal advice."}
