21 CFR § 111.310 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.310 What are the requirements for the laboratory facilities that you use?

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

You must use adequate laboratory facilities to perform whatever testing and examinations are necessary to determine whether:

(a) Components that you use meet specifications;

(b) In-process specifications are met as specified in the master manufacturing record; and

(c) Dietary supplements that you manufacture meet specifications.

← § 111.303 What are the requirements under this subpart J for written procedures?§ 111.315 What are the requirements for laboratory control processes? →