21 CFR 803.56
If I am a manufacturer, in what circumstances must I submit a supplemental or followup report and what are the requirements for such reports?
- Inspections citing it: 58
- Of those classified, ended OAI: 31%
- Last cited: FY2025
Inspections Citing It by Fiscal Year
Sites in and outside the US, FY2017 to Oct 20, 2026.
Regulation Text
eCFR, as of Nov 6, 2026If you are a manufacturer, when you obtain information required under this part that you did not provide because it was not known or was not available when you submitted the initial report, you must submit the supplemental information to us within 30 calendar days of the day that you receive this information. You must submit the supplemental or followup report in accordance with the requirements of § 803.12(a). On a supplemental or followup report, you must:
(a) Indicate that the report being submitted is a supplemental or followup report;
(b) Submit the appropriate identification numbers of the report that you are updating with the supplemental information (e.g., your original manufacturer report number and the user facility or importer report number of any report on which your report was based), if applicable; and
(c) Include only the new, changed, or corrected information.
Recently Cited Sites
Newest inspections citing this section; each opens the site- Sol-Millennium Medical Inc.United States · May 8, 2025
- Maquet Cardiovascular, LLCUnited States · Jul 11, 2024
- Datascope Corp.United States · Jun 15, 2023
- Sakura Seiki Co., Ltd. Chikuma FactoryJapan · Mar 24, 2023
Counts are inspections with posted citations that cite any paragraph of the section, once per inspection, from FDA's Data Dashboard. OAI share is over inspections FDA finally classified. Text from eCFR, the official online CFR. FDA Data Dashboard and eCFR