# UST MFG LLC, Layton, UT – FDA Inspections

Source: https://www.keypedia.com/companies/ust-mfg-llc/22efbde4-964b-4620-8112-219ce00eb4c5

> Inspection records and compliance data for UST MFG LLC in Layton, Utah. 6 FDA inspections on record, last inspected March 06, 2025.

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## Details

- Name: UST MFG LLC
- FEI Number: 3007553306
- Address Line 1: 855 Mccormick Way
- City: Layton
- State: Utah
- Zip Code: 84041
- Country Name: United States
- Address: 855 Mccormick Way, Layton, Utah 84041, United States
- Country: United States

## Related Documents

- FDA Inspection 1262439 - UST MFG LLC - 2025-03-06 — source: FDA, date: March 6, 2025
- FDA Inspection 1262439 - UST MFG LLC - 2025-03-06 — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2025
- [FDA Inspection 1262439 - UST MFG LLC - 2025-03-06](https://www.keypedia.com/records/fda_inspections/ust-mfg-llc/d69460e4-54e1-49f1-b1de-8402311d7476) — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2025
- FDA Inspection 1253851 - UST MFG LLC - 2023-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2023
- FDA Inspection 1253851 - UST MFG LLC - 2023-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2023
- FDA Inspection 1154742 - UST MFG LLC - 2021-07-28 — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2021
- FDA Inspection 1025921 - UST MFG LLC - 2017-08-14 — classification: No Action Indicated (NAI), source: FDA, date: August 14, 2017
- FDA Inspection 1025921 - UST MFG LLC - 2017-08-14 — classification: No Action Indicated (NAI), source: FDA, date: August 14, 2017
- [FDA Inspection 874333 - UST MFG LLC - 2014-04-15](https://www.keypedia.com/records/fda_inspections/ust-mfg-llc/1d3761b9-8043-4f2e-87c9-bcfb154cd925) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 15, 2014
- [FDA Inspection 806187 - UST MFG LLC - 2012-10-31](https://www.keypedia.com/records/fda_inspections/ust-mfg-llc/7677ec78-2475-43c8-9a00-3f8293b65fb3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 31, 2012

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