21 CFR § 226.115 Current Good Manufacturing Practice for Type a Medicated Articles

§ 226.115 Complaint files.

Current through Sep 8, 2026 · Read all of Part 226

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.

← § 226.110 Distribution records.