21 C.F.R. · Food and Drugs
21 C.F.R. § 1.282

What must you do if information changes after you have received confirmation of a prior notice from FDA?

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21 C.F.R. § 1.282 — What must you do if information changes after you have received confirmation of a prior notice from FDA?

§ 1.282 What must you do if information changes after you have received confirmation of a prior notice from FDA? (a)(1) If any of the information required in § 1.281(a), except the information required in: (i) Section 1.281(a)(5)(iii) (quantity), (ii) Section 1.281(a)(11) (anticipated arrival information), or (iii) Section 1.281(a)(17) (planned shipment information), changes after you receive notice that FDA has confirmed your prior notice submission for review, you must resubmit prior notice in accordance with this subpart unless the article of food will not be offered for import or imported into the United States. (2) If any of the information required in § 1.281(b), except the information required in § 1.281(b)(10) (the anticipated date of mailing), changes after you receive notice that FDA has confirmed your prior notice submission for review, you must resubmit prior notice in accordance with this subpart, unless the article of food will not be offered for import or imported into the United States. (b) If you submitted the prior notice via the FDA PNSI, you should cancel the prior notice via the FDA PNSI. (c) If you submitted the prior notice via ABI/ACE/ITDS, you should cancel the prior notice via ACE by requesting that CBP cancel the entry. [73 FR 66402, Nov. 7, 2008, as amended at 82 FR 15629, Mar. 30, 2017] Consequences

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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The regulatory text of 21 C.F.R. § 1.282 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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