# J R Simplot Company, Grand Forks, ND – FDA Inspections

Source: https://www.keypedia.com/companies/j-r-simplot-company/9212858a-e98a-46ef-a03c-4fa25acf23e6

> Inspection records and compliance data for J R Simplot Company in Grand Forks, North Dakota. 8 FDA inspections on record, last inspected June 14, 2022.

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## Details

- Name: J R Simplot Company
- FEI Number: 1720157
- Address Line 1: 3630 Gateway Dr
- City: Grand Forks
- State: North Dakota
- Zip Code: 58203
- Country Name: United States
- Address: 3630 Gateway Dr, Grand Forks, North Dakota 58203, United States
- Country: United States

## Related Documents

- FDA Inspection 1172463 - J R Simplot Company - 2022-06-14 — classification: No Action Indicated (NAI), source: FDA, date: June 14, 2022
- FDA Inspection 1134832 - J R Simplot Company - 2021-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2021
- FDA Inspection 1091772 - J R Simplot Company - 2019-05-22 — source: FDA, date: May 22, 2019
- FDA Inspection 971461 - J R Simplot Company - 2016-04-29 — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2016
- [FDA Inspection 971461 - J R Simplot Company - 2016-04-29](https://www.keypedia.com/records/fda_inspections/j-r-simplot-company/709552fa-34b0-4c66-ad21-c67c5b902588) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2016
- FDA Inspection 836316 - J R Simplot Company - 2013-06-04 — classification: No Action Indicated (NAI), source: FDA, date: June 4, 2013
- FDA Inspection 759867 - J R Simplot Company - 2011-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2011
- FDA Inspection 759867 - J R Simplot Company - 2011-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2011
- FDA Inspection 677154 - J R Simplot Company - 2010-06-24 — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2010
- FDA Inspection 611873 - J R Simplot Company - 2009-09-02 — classification: No Action Indicated (NAI), source: FDA, date: September 2, 2009

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