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FDA Inspection
•Beaumont Products Inc.•November 6, 2012

Beaumont Products Inc. – FDA Inspection, Nov 6, 2012

Record Details

This FDA Inspection record concerns Beaumont Products Inc., with an inspection on November 6, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Beaumont Products Inc.
Inspection Date
November 6, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · a2c17950-1789-4970-88f8-a20af72207fc

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
808984
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

12
  1. 21 CFR 211.58Buildings not maintained in good state of repair
  2. 21 CFR 211.110(a)Control procedures to monitor and validate performance
  3. 21 CFR 211.46(b)Equipment for Environmental Control
  4. 21 CFR 211.25(a)GMP Training Frequency
  5. 21 CFR 211.170(b)Annual visual exams of drug products
  6. 21 CFR 211.25(c)Inadequate number of personnel
  7. 21 CFR 211.182Personnel dating/signing equipment log
  8. 21 CFR 211.22(d)Procedures not in writing, fully followed
  9. 21 CFR 211.180(e)(2)Items to cover on annual reviews
  10. 21 CFR 211.67(b)Written procedures fail to include

Showing 10 of 12 citations.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Beaumont Products Inc.

5
DateClassificationOfficeProject area
July 29, 2025Not classifiedAtlanta District Office
September 7, 2023NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
October 8, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 22, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 22, 2010NAICenter for Food Safety and Applied NutritionColors 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 947720 - 2015-10-22
  • FDA Inspection 648614 - 2010-01-22

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