# Dierbergs Markets, Inc., Bridgeton, MO – FDA Inspections

Source: https://www.keypedia.com/companies/dierbergs-markets-inc/83fac19a-0ba0-4f98-ab81-d4b1d6ed5b16

> Inspection records and compliance data for Dierbergs Markets, Inc. in Bridgeton, Missouri. 8 FDA inspections on record, 2 Form 483s, last inspected December 17, 2025.

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## Details

- Name: Dierbergs Markets, Inc.
- FEI Number: 3004694541
- Address Line 1: 3400b Hollenberg Dr
- City: Bridgeton
- State: Missouri
- Zip Code: 63044
- Country Name: United States
- Address: 3400b Hollenberg Dr, Bridgeton, Missouri 63044, United States
- Country: United States

## Related Documents

- FDA Inspection 1296600 - Dierbergs Markets, Inc. - 2025-12-17 — source: FDA, date: December 17, 2025
- FDA Inspection 1296600 - Dierbergs Markets, Inc. - 2025-12-17 — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2025
- FDA Inspection 1258777 - Dierbergs Markets, Inc. - 2025-01-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2025
- [FDA Inspection 1258777 - Dierbergs Markets, Inc. - 2025-01-21](https://www.keypedia.com/records/fda_inspections/dierbergs-markets-inc/e67b826e-88b9-41d1-8e57-88a2663bb086) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2025
- FDA Inspection 1258777 - Dierbergs Markets, Inc. - 2025-01-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2025
- FDA Inspection 1223255 - Dierbergs Markets, Inc. - 2023-11-08 — source: FDA, date: November 8, 2023
- FDA Inspection 1181935 - Dierbergs Markets, Inc. - 2022-10-06 — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2022
- FDA Inspection 1181935 - Dierbergs Markets, Inc. - 2022-10-06 — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2022
- FDA Inspection 1042723 - Dierbergs Markets, Inc. - 2018-01-12 — classification: No Action Indicated (NAI), source: FDA, date: January 12, 2018
- FDA Inspection 1042709 - Dierbergs Markets, Inc. - 2018-01-10 — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2018

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