21 C.F.R. · Food and Drugs
21 C.F.R. § 1.1400

What procedures apply if FDA tentatively determines that modified requirements or an exemption should be revised or revoked?

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 1.1400 — What procedures apply if FDA tentatively determines that modified requirements or an exemption should be revised or revoked?

§ 1.1400 What procedures apply if FDA tentatively determines that modified requirements or an exemption should be revised or revoked? (a) If FDA tentatively determines that we should revise or revoke modified requirements or an exemption, we will provide the following notifications: (1) We will notify the person that originally requested the modified requirements or exemption (if we adopted modified requirements or granted an exemption in response to a petition) in writing at the address identified in the petition; and (2) We will publish a notice in the Federal Register of our tentative determination that the modified requirements or exemption should be revised or revoked and the reasons for our tentative decision. The notice will establish a public docket so that interested persons may submit written comments on our tentative determination. (b) After considering any comments timely submitted, we will publish a notice in the Federal Register of our decision whether to revise or revoke the modified requirements or exemption and the reasons for the decision. If we do revise or revoke the modified requirements or exemption, the effective date of the decision will be 1 year after the date of publication of the notice, unless otherwise stated in the notice. Waivers

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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21 C.F.R. § 1.1400
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The regulatory text of 21 C.F.R. § 1.1400 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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