{"data":{"id":"us/21-cfr-213.89","jurisdiction":"us","citation":"21 CFR 213.89","heading":"Rejected components, incoming designated medical gases, and medical gas containers and closures.","body":"Rejected components, incoming designated medical gases, and medical gas containers and closures shall be identified and controlled under a quarantine system designed to prevent their use in manufacturing or processing operations for which they are unsuitable and shall be documented and assessed.","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 E—Control of Incoming Designated Medical Gas, Components, and Medical Gas Containers and Closures"],"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":"f147df4bbb628ac612763edb07d9769194af128f571168ddbefe3ae02a459fb9","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-213.84","next":"us/21-cfr-213.94"},"notice":"GroundRules: Original legal text. Not legal advice."}