{"data":{"id":"us/21-cfr-211.105","jurisdiction":"us","citation":"21 CFR 211.105","heading":"Equipment identification.","body":"(a) All compounding and storage containers, processing lines, and major equipment used during the production of a batch of a drug product shall be properly identified at all times to indicate their contents and, when necessary, the phase of processing of the batch.\n(b) Major equipment shall be identified by a distinctive identification number or code that shall be recorded in the batch production record to show the specific equipment used in the manufacture of each batch of a drug product. In cases where only one of a particular type of equipment exists in a manufacturing facility, the name of the equipment may be used in lieu of a distinctive identification number or code.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS","Subpart F—Production and Process Controls"],"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":"aa5116acd4895e8624bcb9211db64648bd2944e55cbe8cd5a8f47f38647999fb","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-211.103","next":"us/21-cfr-211.110"},"notice":"GroundRules: Original legal text. Not legal advice."}