21 CFR § 111.375 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.375 Under this subpart K, what records must you make and keep?

Current through Sep 8, 2026 · Read all of Part 111

(a) You must make and keep records required under this subpart K in accordance with subpart P of this part.

(b) You must make and keep records of the written procedures for manufacturing operations.

← § 111.370 What requirements apply to rejected dietary supplements?§ 111.403 What are the requirements under this subpart L for written procedures? →