# John Kuhni Sons, Inc., Levan, UT – FDA Inspections

Source: https://www.keypedia.com/companies/john-kuhni-sons-inc/185470bd-a25d-4756-b31a-2ea5ccf15ff3

> Inspection records and compliance data for John Kuhni Sons, Inc. in Levan, Utah. 10 FDA inspections on record, last inspected January 30, 2018.

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## Details

- Name: John Kuhni Sons, Inc.
- FEI Number: 1780166
- Address Line 1: 6480 West Mills Road
- City: Levan
- State: Utah
- Zip Code: 84639
- Country Name: United States
- Address: 6480 West Mills Road, Levan, Utah 84639, United States
- Country: United States

## Related Documents

- FDA Inspection 1053325 - John Kuhni Sons, Inc. - 2018-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2018
- FDA Inspection 996648 - John Kuhni Sons, Inc. - 2016-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2016
- FDA Inspection 948761 - John Kuhni Sons, Inc. - 2015-10-22 — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2015
- FDA Inspection 899529 - John Kuhni Sons, Inc. - 2014-10-06 — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2014
- FDA Inspection 859664 - John Kuhni Sons, Inc. - 2013-12-19 — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2013
- FDA Inspection 825965 - John Kuhni Sons, Inc. - 2013-02-27 — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2013
- FDA Inspection 782010 - John Kuhni Sons, Inc. - 2012-05-17 — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2012
- [FDA Inspection 739051 - John Kuhni Sons, Inc. - 2011-08-09](https://www.keypedia.com/records/fda_inspections/john-kuhni-sons-inc/fa126e59-c4f2-45c7-b860-7e84e39b7481) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 9, 2011
- FDA Inspection 637981 - John Kuhni Sons, Inc. - 2010-01-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 8, 2010
- FDA Inspection 597955 - John Kuhni Sons, Inc. - 2009-07-09 — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2009

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