# Dakota Specialty Milling, Inc, Fargo, ND – FDA Inspections

Source: https://www.keypedia.com/companies/dakota-specialty-milling-inc/fffb9bfd-911b-4829-b801-6722e0be0276

> Inspection records and compliance data for Dakota Specialty Milling, Inc in Fargo, North Dakota. 9 FDA inspections on record, last inspected January 31, 2024.

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## Details

- Name: Dakota Specialty Milling, Inc
- FEI Number: 2130865
- Address Line 1: 4014 15th Ave N
- City: Fargo
- State: North Dakota
- Zip Code: 58102
- Country Name: United States
- Address: 4014 15th Ave N, Fargo, North Dakota 58102, United States
- Country: United States

## Related Documents

- FDA Inspection 1228297 - Dakota Specialty Milling, Inc - 2024-01-31 — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2024
- FDA Inspection 1137012 - Dakota Specialty Milling, Inc - 2021-02-17 — classification: No Action Indicated (NAI), source: FDA, date: February 17, 2021
- FDA Inspection 1099468 - Dakota Specialty Milling, Inc - 2019-07-16 — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2019
- FDA Inspection 1016871 - Dakota Specialty Milling, Inc - 2017-06-27 — classification: No Action Indicated (NAI), source: FDA, date: June 27, 2017
- FDA Inspection 896583 - Dakota Specialty Milling, Inc - 2014-09-09 — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2014
- FDA Inspection 831275 - Dakota Specialty Milling, Inc - 2013-05-09 — classification: No Action Indicated (NAI), source: FDA, date: May 9, 2013
- FDA Inspection 831275 - Dakota Specialty Milling, Inc - 2013-05-09 — classification: No Action Indicated (NAI), source: FDA, date: May 9, 2013
- FDA Inspection 749788 - Dakota Specialty Milling, Inc - 2011-10-17 — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2011
- FDA Inspection 666763 - Dakota Specialty Milling, Inc - 2010-06-15 — classification: No Action Indicated (NAI), source: FDA, date: June 15, 2010
- FDA Inspection 595715 - Dakota Specialty Milling, Inc - 2009-07-08 — classification: No Action Indicated (NAI), source: FDA, date: July 8, 2009

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