FDA Inspection
Beaumont Products Inc.Beaumont Products Inc. – FDA Inspection, Oct 22, 2015
Record Details
This FDA Inspection record concerns Beaumont Products Inc., with an inspection on October 22, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Beaumont Products Inc.
- Inspection Date
- October 22, 2015
- Product Type
- Drugs
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ID · bfc553fb-6629-464d-8de5-4d4ea42fdda4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 947720
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.110(a)Control procedures to monitor and validate performance
- 21 CFR 211.142(a)Quarantine - actual practice
- 21 CFR 211.111Establishment of time limitations
- 21 CFR 211.180(e)(2)Items to cover on annual reviews
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Beaumont Products Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| July 29, 2025 | Not classified | Atlanta District Office | |
| September 7, 2023 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| October 8, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 6, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2010 | NAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
Other documents for Beaumont Products Inc.
- FDA Inspection 1277387 - 2025-07-29
- FDA Inspection 1217683 - 2023-09-07
- FDA Inspection 1106846 - 2019-10-08
- FDA Inspection 808984 - 2012-11-06
- FDA Inspection 648614 - 2010-01-22
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