# Burch Food Services, Inc, Sikeston, MO – FDA Inspections

Source: https://www.keypedia.com/companies/burch-food-services-inc/601b70b4-2c6e-4dde-bd52-6d8c8ab64da5

> Inspection records and compliance data for Burch Food Services, Inc in Sikeston, Missouri. 8 FDA inspections on record, 2 Form 483s, last inspected August 06, 2025.

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## Details

- Name: Burch Food Services, Inc
- FEI Number: 1000219036
- Address Line 1: 108 Stallcup Dr
- City: Sikeston
- State: Missouri
- Zip Code: 63801
- Country Name: United States
- Address: 108 Stallcup Dr, Sikeston, Missouri 63801, United States
- Country: United States

## Related Documents

- FDA Inspection 1278711 - Burch Food Services, Inc - 2025-08-06 — source: FDA, date: August 6, 2025
- FDA Inspection 1236896 - Burch Food Services, Inc - 2024-03-27 — classification: No Action Indicated (NAI), source: FDA, date: March 27, 2024
- [FDA Inspection 1089503 - Burch Food Services, Inc - 2019-03-25](https://www.keypedia.com/records/fda_inspections/burch-food-services-inc/65e019a4-333a-4fdf-bc8e-120e6b4db459) — source: FDA, date: March 25, 2019
- [FDA Inspection 1059453 - Burch Food Services, Inc - 2018-06-01](https://www.keypedia.com/records/fda_inspections/burch-food-services-inc/66b390c3-8c95-4164-a7d9-05bd6bb4906c) — source: FDA, date: June 1, 2018
- [FDA Inspection 987384 - Burch Food Services, Inc - 2016-08-04](https://www.keypedia.com/records/fda_inspections/burch-food-services-inc/9445dc47-e778-467a-baac-fc3683092d85) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 4, 2016
- [FDA Inspection 762349 - Burch Food Services, Inc - 2012-01-10](https://www.keypedia.com/records/fda_inspections/burch-food-services-inc/605ce6ed-849b-4a74-b21c-20d779ef36f3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 10, 2012
- FDA Inspection 748993 - Burch Food Services, Inc - 2011-09-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2011
- FDA Inspection 714447 - Burch Food Services, Inc - 2011-03-10 — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2011

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