part_subject: "CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS"
subpart_code: "D"
subpart_subject: "Equipment and Utensils"
section_number: "111.25"
section_subject: "What are the requirements under this subpart D for written procedures?"
cfr_reference: "21 CFR 111.25"
title_name: "Title 21"
title_subject: "Food and Drugs"
parts_covered: "Parts 100 to 169"
revised_date: "Revised as of April 1, 2019"
publication_date: "As of April 1, 2019"
contains_description: "Containing a codification of documents of general applicability and future effect"
publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"
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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.