# Drayton Foods, LLC, Fargo, ND – FDA Inspections

Source: https://www.keypedia.com/companies/drayton-foods-llc/5c296eef-1136-4bdf-9991-2a307fc6dec7

> Inspection records and compliance data for Drayton Foods, LLC in Fargo, North Dakota. 7 FDA inspections on record, 1 Form 483, last inspected July 25, 2024.

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## Details

- Name: Drayton Foods, LLC
- FEI Number: 3000717458
- Address Line 1: 1307 39th St N
- City: Fargo
- State: North Dakota
- Zip Code: 58102
- Country Name: United States
- Address: 1307 39th St N, Fargo, North Dakota 58102, United States
- Country: United States

## Related Documents

- FDA Inspection 1244884 - Drayton Foods, LLC - 2024-07-25 — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2024
- [FDA Inspection 1135159 - Drayton Foods, LLC - 2021-01-28](https://www.keypedia.com/records/fda_inspections/drayton-foods-llc/427c6ace-6cf0-47a6-9cbb-4c63b2f05a3c) — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2021
- [FDA Inspection 1060027 - Drayton Foods, LLC - 2018-07-18](https://www.keypedia.com/records/fda_inspections/drayton-foods-llc/8cc1f5fa-f734-4cea-8176-c8fe1cc6cc26) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 18, 2018
- [FDA Inspection 917912 - Drayton Foods, LLC - 2015-03-12](https://www.keypedia.com/records/fda_inspections/drayton-foods-llc/087126b8-908e-4232-97a2-c65b3e342e43) — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2015
- [FDA Inspection 768911 - Drayton Foods, LLC - 2012-02-23](https://www.keypedia.com/records/fda_inspections/drayton-foods-llc/73614caf-5e50-427a-bccf-39bdffc31fc7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 23, 2012
- [FDA Inspection 657671 - Drayton Foods, LLC - 2010-04-09](https://www.keypedia.com/records/fda_inspections/drayton-foods-llc/09cfde9b-ca50-4457-b52b-ca1b89bb053e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 9, 2010
- FDA Inspection 601925 - Drayton Foods, LLC - 2009-07-23 — classification: No Action Indicated (NAI), source: FDA, date: July 23, 2009

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