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, p m u m us m u m an M E E T M E E R N___5I Serb Form 374 ta SHU. S. NUCLEI AR CE!oratory Commission| I l Gig. Ghv6. Byproduct, source, and/or special nuclear material)k! A. Any byproduct|section

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What is 21 usc 374?

21 usc 374 refers to the United States Code section regarding inspection of factories and records by the Food and Drug Administration (FDA).

Who is required to file 21 usc 374?

Manufacturers, packers, and distributors of drugs, devices, or cosmetics are required to file 21 usc 374.

How to fill out 21 usc 374?

To fill out 21 usc 374, the required information must be provided as requested by the FDA, including details about the facility, products, and the required records.

What is the purpose of 21 usc 374?

The purpose of 21 usc 374 is to ensure that drugs, devices, and cosmetics distributed in the United States are manufactured in compliance with FDA regulations for safety and quality.

What information must be reported on 21 usc 374?

Information such as facility details, product details, manufacturing processes, quality control measures, and distribution records must be reported on 21 usc 374.

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