# Bimbo Bakeries USA, Inc, Owensboro, KY – FDA Inspections

Source: https://www.keypedia.com/companies/bimbo-bakeries-usa-inc/ac76525d-536f-4401-bad6-bf75cffbb004

> Inspection records and compliance data for Bimbo Bakeries USA, Inc in Owensboro, Kentucky. 5 FDA inspections on record, last inspected December 23, 2025.

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## Details

- Name: Bimbo Bakeries USA, Inc
- FEI Number: 1021578
- Address Line 1: 335 E 25th St
- City: Owensboro
- State: Kentucky
- Zip Code: 42303
- Country Name: United States
- Address: 335 E 25th St, Owensboro, Kentucky 42303, United States
- Country: United States

## Related Documents

- FDA Inspection 1283797 - Bimbo Bakeries USA, Inc - 2025-12-23 — source: FDA, date: December 23, 2025
- FDA Inspection 1013038 - Bimbo Bakeries USA, Inc - 2017-05-02 — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2017
- FDA Inspection 1013038 - Bimbo Bakeries USA, Inc - 2017-05-02 — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2017
- FDA Inspection 836538 - Bimbo Bakeries USA, Inc - 2013-05-01 — classification: No Action Indicated (NAI), source: FDA, date: May 1, 2013
- FDA Inspection 836538 - Bimbo Bakeries USA, Inc - 2013-05-01 — classification: No Action Indicated (NAI), source: FDA, date: May 1, 2013
- FDA Inspection 700116 - Bimbo Bakeries USA, Inc - 2010-11-18 — classification: No Action Indicated (NAI), source: FDA, date: November 18, 2010
- [FDA Inspection 700116 - Bimbo Bakeries USA, Inc - 2010-11-18](https://www.keypedia.com/records/fda_inspections/bimbo-bakeries-usa-inc/d3bbc229-798a-4d0e-91d6-2b6d4792768e) — classification: No Action Indicated (NAI), source: FDA, date: November 18, 2010
- FDA Inspection 700116 - Bimbo Bakeries USA, Inc - 2010-11-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2010
- FDA Inspection 651438 - Bimbo Bakeries USA, Inc - 2010-02-04 — classification: No Action Indicated (NAI), source: FDA, date: February 4, 2010
- FDA Inspection 651438 - Bimbo Bakeries USA, Inc - 2010-02-04 — classification: No Action Indicated (NAI), source: FDA, date: February 4, 2010

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