21 CFR 111.25
§ 111.25 What are the requirements under this subpart D for written procedures?
United States · 21 CFR — Food and Drugs · Status: effective
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- Citation
- 21 CFR 111.25, § 111.25 What are the requirements under this subpart D for written procedures?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/84139
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Full text
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.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.