# Western Nut Company, Inc., Salt Lake City, UT – FDA Inspections

Source: https://www.keypedia.com/companies/western-nut-company-inc/2e2323c7-9104-4e22-98ad-ba52b7eb410c

> Inspection records and compliance data for Western Nut Company, Inc. in Salt Lake City, Utah. 6 FDA inspections on record, 2 Form 483s, last inspected December 17, 2025.

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## Details

- Name: Western Nut Company, Inc.
- FEI Number: 1713396
- Address Line 1: 434 S 300 W
- City: Salt Lake City
- State: Utah
- Zip Code: 84101
- Country Name: United States
- Address: 434 S 300 W, Salt Lake City, Utah 84101, United States
- Country: United States

## Related Documents

- FDA Inspection 1297086 - Western Nut Company, Inc. - 2025-12-17 — source: FDA, date: December 17, 2025
- FDA Inspection 1297086 - Western Nut Company, Inc. - 2025-12-17 — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2025
- [FDA Inspection 1217530 - Western Nut Company, Inc. - 2023-09-11](https://www.keypedia.com/records/fda_inspections/western-nut-company-inc/d6e187ac-253c-47d2-a868-2ce14508c272) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 11, 2023
- [FDA Inspection 1102500 - Western Nut Company, Inc. - 2019-09-20](https://www.keypedia.com/records/fda_inspections/western-nut-company-inc/cdcd1ce9-9ede-4b67-af13-030c7999c27c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 20, 2019
- FDA Inspection 1000603 - Western Nut Company, Inc. - 2017-01-06 — classification: No Action Indicated (NAI), source: FDA, date: January 6, 2017
- [FDA Inspection 881332 - Western Nut Company, Inc. - 2014-06-03](https://www.keypedia.com/records/fda_inspections/western-nut-company-inc/d4f8f44e-5cec-4c0d-86e4-e9aba9307f21) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 3, 2014
- FDA Inspection 553821 - Western Nut Company, Inc. - 2008-12-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 29, 2008
- FDA Inspection 553821 - Western Nut Company, Inc. - 2008-12-29 — classification: No Action Indicated (NAI), source: FDA, date: December 29, 2008

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