# Burnette Foods, Inc. Plant # 3, East Jordan, MI – FDA Inspections

Source: https://www.keypedia.com/companies/burnette-foods-inc-plant-3/d21043c6-9ae1-4085-b695-07801c66d40c

> Inspection records and compliance data for Burnette Foods, Inc. Plant # 3 in East Jordan, Michigan. 6 FDA inspections on record, 2 Form 483s, last inspected October 19, 2023.

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## Details

- Name: Burnette Foods, Inc. Plant # 3
- FEI Number: 1810529
- Address Line 1: 200 State St
- City: East Jordan
- State: Michigan
- Zip Code: 49727
- Country Name: United States
- Address: 200 State St, East Jordan, Michigan 49727, United States
- Country: United States

## Related Documents

- [FDA Inspection 1221674 - Burnette Foods, Inc. Plant # 3 - 2023-10-19](https://www.keypedia.com/records/fda_inspections/burnette-foods-inc-plant-3/44009a7d-be87-430a-b636-0f8caa5f35eb) — source: FDA, date: October 19, 2023
- [FDA Inspection 1056368 - Burnette Foods, Inc. Plant # 3 - 2018-06-21](https://www.keypedia.com/records/fda_inspections/burnette-foods-inc-plant-3/4038f4bc-a442-45f9-95ca-ece86ad2a941) — source: FDA, date: June 21, 2018
- FDA Inspection 879646 - Burnette Foods, Inc. Plant # 3 - 2014-05-22 — classification: No Action Indicated (NAI), source: FDA, date: May 22, 2014
- FDA Inspection 772449 - Burnette Foods, Inc. Plant # 3 - 2012-02-24 — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2012
- [FDA Inspection 675594 - Burnette Foods, Inc. Plant # 3 - 2010-08-11](https://www.keypedia.com/records/fda_inspections/burnette-foods-inc-plant-3/d4fe5b2a-b5e7-440f-a244-8000d550e8f3) — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2010
- FDA Inspection 675594 - Burnette Foods, Inc. Plant # 3 - 2010-08-11 — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2010
- FDA Inspection 675594 - Burnette Foods, Inc. Plant # 3 - 2010-08-11 — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2010
- FDA Inspection 615225 - Burnette Foods, Inc. Plant # 3 - 2009-09-23 — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2009

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