{"data":{"id":"us/21-cfr-226.115","jurisdiction":"us","citation":"21 CFR 226.115","heading":"Complaint files.","body":"Records shall be maintained for a period of 2 years of all written or verbal complaints concerning the safety or efficacy of each Type A medicated article(s). Complaints shall be evaluated by competent and responsible personnel and, where indicated, appropriate action shall be taken. The record shall indicate the evaluation and the action.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES","Subpart E—Records and Reports"],"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":"e2b0e26bd3a1124c283e46fa6d2d061a105e099a607cefaf75f4c6c1e2a3bc43","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-226.110","next":"us/21-cfr-230.1"},"notice":"GroundRules: Original legal text. Not legal advice."}