# Bimbo Bakeries USA, Bellevue, NE – FDA Inspections

Source: https://www.keypedia.com/companies/bimbo-bakeries-usa/0e00bdff-a0ca-4731-b6cb-2256b0084ef6

> Inspection records and compliance data for Bimbo Bakeries USA in Bellevue, Nebraska. 6 FDA inspections on record, 1 Form 483, last inspected November 29, 2022.

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## Details

- Name: Bimbo Bakeries USA
- FEI Number: 1921040
- Address Line 1: 1310 Fort Crook Rd N
- City: Bellevue
- State: Nebraska
- Zip Code: 68005
- Country Name: United States
- Address: 1310 Fort Crook Rd N, Bellevue, Nebraska 68005, United States
- Country: United States

## Related Documents

- FDA Inspection 1192768 - Bimbo Bakeries USA - 2022-11-29 — classification: No Action Indicated (NAI), source: FDA, date: November 29, 2022
- FDA Inspection 1178625 - Bimbo Bakeries USA - 2022-08-25 — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2022
- FDA Inspection 1100859 - Bimbo Bakeries USA - 2019-07-12 — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2019
- FDA Inspection 1100859 - Bimbo Bakeries USA - 2019-07-12 — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2019
- [FDA Inspection 994270 - Bimbo Bakeries USA - 2016-11-16](https://www.keypedia.com/records/fda_inspections/bimbo-bakeries-usa/135b256e-fdba-4cb0-97ad-c87d51a3d416) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 16, 2016
- FDA Inspection 913371 - Bimbo Bakeries USA - 2015-02-10 — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2015
- FDA Inspection 773441 - Bimbo Bakeries USA - 2012-03-09 — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2012
- FDA Inspection 773441 - Bimbo Bakeries USA - 2012-03-09 — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2012
- FDA Inspection 773441 - Bimbo Bakeries USA - 2012-03-09 — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2012
- FDA Inspection 773441 - Bimbo Bakeries USA - 2012-03-09 — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2012

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