FDA Inspection
Trividia Manufacturing Solutions, Inc.Trividia Manufacturing Solutions, Inc. – FDA Inspection, Mar 6, 2025
Record Details
This FDA Inspection record concerns Trividia Manufacturing Solutions, Inc., with an inspection on March 6, 2025, issued by the New England District Office, covering human drugs.
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ID · e3f4ecbd-8714-4bab-8e93-62be71e1c962
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1263186
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.25(a)Training , Education , Experience overall
- 21 CFR 211.198(a)Complaint Handling Procedure
- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.194(a)(2)Laboratory Test Method Verification
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Trividia Manufacturing Solutions, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| May 3, 2023 | NAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| November 7, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 24, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 9, 2017 | NAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| June 5, 2014 | VAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
Other documents for Trividia Manufacturing Solutions, Inc.
- FDA Inspection 1206742 - 2023-05-03
- FDA Inspection 1071302 - 2018-11-07
- FDA Inspection 1063417 - 2018-08-24
- FDA Inspection 1026178 - 2017-08-09
- FDA Inspection 882410 - 2014-06-05
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