# Bowie Produce Company, Inc., Landover, MD – FDA Inspections

Source: https://www.keypedia.com/companies/bowie-produce-company-inc/f8bdaef4-2fe1-4de4-a6c2-2c93cfb99eb0

> Inspection records and compliance data for Bowie Produce Company, Inc. in Landover, Maryland. 8 FDA inspections on record, last inspected September 04, 2025.

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## Details

- Name: Bowie Produce Company, Inc.
- FEI Number: 1000122963
- Address Line 1: 2020 Beaver Rd
- City: Landover
- State: Maryland
- Zip Code: 20785
- Country Name: United States
- Address: 2020 Beaver Rd, Landover, Maryland 20785, United States
- Country: United States

## Related Documents

- FDA Inspection 1281279 - Bowie Produce Company, Inc. - 2025-09-04 — source: FDA, date: September 4, 2025
- FDA Inspection 1226478 - Bowie Produce Company, Inc. - 2023-11-30 — source: FDA, date: November 30, 2023
- FDA Inspection 1109455 - Bowie Produce Company, Inc. - 2019-10-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2019
- [FDA Inspection 1109455 - Bowie Produce Company, Inc. - 2019-10-31](https://www.keypedia.com/records/fda_inspections/bowie-produce-company-inc/9795e5fb-a5f4-4645-9ae7-bfeedafc187f) — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2019
- FDA Inspection 1014744 - Bowie Produce Company, Inc. - 2017-05-23 — source: FDA, date: May 23, 2017
- FDA Inspection 913476 - Bowie Produce Company, Inc. - 2015-02-11 — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2015
- FDA Inspection 832720 - Bowie Produce Company, Inc. - 2013-05-22 — classification: No Action Indicated (NAI), source: FDA, date: May 22, 2013
- [FDA Inspection 654643 - Bowie Produce Company, Inc. - 2010-03-12](https://www.keypedia.com/records/fda_inspections/bowie-produce-company-inc/7cfd4050-2c50-4edd-8252-33369374c20e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 12, 2010
- FDA Inspection 556130 - Bowie Produce Company, Inc. - 2009-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2009

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