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21 CFR 1.700

§ 1.700 Who is subject to a user fee under this subpart?

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 1.700, § 1.700 Who is subject to a user fee under this subpart?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/82872
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(a) Accreditation bodies submitting applications or renewal applications for recognition in the third-party certification program; (b) Recognized accreditation bodies participating in the third-party certification program; (c) Third-party certification bodies submitting applications or renewal applications for direct accreditation; and (d) Accredited third-party certification bodies (whether accredited by recognized accreditation bodies or by FDA through direct accreditation) participating in the third-party certification program.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.