21 CFR § 111.25 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.25 What are the requirements under this subpart D for written procedures?

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

You must establish and follow written procedures for fulfilling the requirements of this subpart D, including written procedures for:

(a) Calibrating instruments and controls that you use in manufacturing or testing a component or dietary supplement;

(b) Calibrating, inspecting, and checking automated, mechanical, and electronic equipment; and

(c) Maintaining, cleaning, and sanitizing, as necessary, all equipment, utensils, and any other contact surfaces that are used to manufacture, package, label, or hold components or dietary supplements.

← § 111.23 Under this subpart C, what records must you make and keep?§ 111.27 What requirements apply to the equipment and utensils that you use? →