21 CFR § 111.430 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.430 Under this subpart L, 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 L in accordance with subpart P of this part.

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

← § 111.425 What requirements apply to a packaged and labeled dietary supplement that is rejected for distribution?§ 111.453 What are the requirements under this subpart for M written procedures? →