# Beaumont Products Inc., Kennesaw, GA – FDA Inspections

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

> Inspection records and compliance data for Beaumont Products Inc. in Kennesaw, Georgia. 6 FDA inspections on record, last inspected July 29, 2025.

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## Details

- Name: Beaumont Products Inc.
- FEI Number: 3000038524
- Address Line 1: 1560 Big Shanty Dr Nw
- City: Kennesaw
- State: Georgia
- Zip Code: 30144
- Country Name: United States
- Address: 1560 Big Shanty Dr Nw, Kennesaw, Georgia 30144, United States
- Country: United States

## Related Documents

- FDA Inspection 1277387 - Beaumont Products Inc. - 2025-07-29 — source: FDA, date: July 29, 2025
- FDA Inspection 1217683 - Beaumont Products Inc. - 2023-09-07 — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2023
- FDA Inspection 1106846 - Beaumont Products Inc. - 2019-10-08 — classification: No Action Indicated (NAI), source: FDA, date: October 8, 2019
- FDA Inspection 947720 - Beaumont Products Inc. - 2015-10-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2015
- [FDA Inspection 947720 - Beaumont Products Inc. - 2015-10-22](https://www.keypedia.com/records/fda_inspections/beaumont-products-inc/bfc553fb-6629-464d-8de5-4d4ea42fdda4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2015
- FDA Inspection 808984 - Beaumont Products Inc. - 2012-11-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 6, 2012
- [FDA Inspection 808984 - Beaumont Products Inc. - 2012-11-06](https://www.keypedia.com/records/fda_inspections/beaumont-products-inc/a2c17950-1789-4970-88f8-a20af72207fc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 6, 2012
- FDA Inspection 648614 - Beaumont Products Inc. - 2010-01-22 — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2010
- FDA Inspection 648614 - Beaumont Products Inc. - 2010-01-22 — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2010
- FDA Inspection 648614 - Beaumont Products Inc. - 2010-01-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2010

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