# Bowman Andros Products, LLC, Mount Jackson, VA – FDA Inspections

Source: https://www.keypedia.com/companies/bowman-andros-products-llc/3dcf9b52-d0c7-4ecb-8982-d2b355478d1a

> Inspection records and compliance data for Bowman Andros Products, LLC in Mount Jackson, Virginia. 8 FDA inspections on record, 1 Form 483, last inspected May 21, 2025.

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## Details

- Name: Bowman Andros Products, LLC
- FEI Number: 1110395
- Address Line 1: 10119 Old Valley Pike
- City: Mount Jackson
- State: Virginia
- Zip Code: 22842
- Country Name: United States
- Address: 10119 Old Valley Pike, Mount Jackson, Virginia 22842, United States
- Country: United States

## Related Documents

- FDA Inspection 1270964 - Bowman Andros Products, LLC - 2025-05-21 — source: FDA, date: May 21, 2025
- FDA Inspection 1270964 - Bowman Andros Products, LLC - 2025-05-21 — classification: No Action Indicated (NAI), source: FDA, date: May 21, 2025
- FDA Inspection 1242783 - Bowman Andros Products, LLC - 2024-06-12 — source: FDA, date: June 12, 2024
- FDA Inspection 1110233 - Bowman Andros Products, LLC - 2019-08-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 2, 2019
- FDA Inspection 1058266 - Bowman Andros Products, LLC - 2018-05-31 — source: FDA, date: May 31, 2018
- [FDA Inspection 1005975 - Bowman Andros Products, LLC - 2017-02-23](https://www.keypedia.com/records/fda_inspections/bowman-andros-products-llc/d285dfe3-b69c-431f-b5d8-300d11da2626) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 23, 2017
- FDA Inspection 946879 - Bowman Andros Products, LLC - 2015-09-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 10, 2015
- FDA Inspection 946879 - Bowman Andros Products, LLC - 2015-09-10 — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2015
- FDA Inspection 668052 - Bowman Andros Products, LLC - 2010-06-21 — classification: No Action Indicated (NAI), source: FDA, date: June 21, 2010
- FDA Inspection 579304 - Bowman Andros Products, LLC - 2009-04-28 — classification: No Action Indicated (NAI), source: FDA, date: April 28, 2009

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