subchapter_subject: "ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS"
part_code: "510"
part_subject: "NEW ANIMAL DRUGS"
subpart_code: "D"
subpart_subject: "Records and Reports"
section_number: "510.305"
section_subject: "Maintenance of copies of approved medicated feed mill licenses to manufacture animal feed bearing or containing new animal drugs."
cfr_reference: "21 CFR 510.305"
title_name: "Title 21"
title_subject: "Food and Drugs"
parts_covered: "Parts 500 to 599"
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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Each applicant shall maintain in a single accessible location:
(a)A copy of the approved medicated feed mill license (Form FDA 3448) on the premises of the manufacturing establishment; and
(b)Approved or index listed labeling for each Type B and/or Type C feed being manufactured on the premises of the manufacturing establishment or the facility where the feed labels are generated.