# Beaumont Products Inc. – FDA Inspection, Oct 22, 2015

Source: https://www.keypedia.com/records/fda_inspections/beaumont-products-inc/bfc553fb-6629-464d-8de5-4d4ea42fdda4
Source feed: FDA_Inspections

> FDA inspection 947720 of Beaumont Products Inc., October 22, 2015. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 211. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 947720
- Company Name: Beaumont Products Inc.
- Inspection Date: 2015-10-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 4

## Related Documents

- FDA Inspection 1277387 - 2025-07-29
- FDA Inspection 1217683 - 2023-09-07
- FDA Inspection 1106846 - 2019-10-08
- [FDA Inspection 808984 - 2012-11-06](https://www.keypedia.com/records/fda_inspections/beaumont-products-inc/a2c17950-1789-4970-88f8-a20af72207fc)
- FDA Inspection 648614 - 2010-01-22

Company: https://www.keypedia.com/companies/beaumont-products-inc/fe1f1cf6-9148-4c16-a764-4537d52c995b

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
