# Kentec Medical, Inc, Irvine, CA – FDA Inspections

Source: https://www.keypedia.com/companies/kentec-medical-inc/84a3c6bd-182a-4acd-bf51-a7482ed87bd7

> Inspection records and compliance data for Kentec Medical, Inc in Irvine, California. 5 FDA inspections on record, 1 Form 483, last inspected July 30, 2018.

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## Details

- Name: Kentec Medical, Inc
- FEI Number: 2080225
- Address Line 1: 17871 Fitch
- City: Irvine
- State: California
- Zip Code: 92614
- Country Name: United States
- Address: 17871 Fitch, Irvine, California 92614, United States
- Country: United States

## Related Documents

- [483 - Kentec Medical, Inc - 2018-07-30](https://www.keypedia.com/records/483/kentec-medical-inc/5b953747-711d-4b2a-88ae-d800f6303327) — source: FDA, date: July 30, 2018
- FDA Inspection 1060879 - Kentec Medical, Inc - 2018-07-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 30, 2018
- [FDA Inspection 1060879 - Kentec Medical, Inc - 2018-07-30](https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/53a53752-8517-4022-8a6e-43817f29509a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 30, 2018
- FDA Inspection 928285 - Kentec Medical, Inc - 2015-05-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 11, 2015
- FDA Inspection 897383 - Kentec Medical, Inc - 2014-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2014
- [FDA Inspection 897383 - Kentec Medical, Inc - 2014-09-24](https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/bd5ba38e-f756-41fa-a386-defecb57535c) — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2014
- FDA Inspection 803967 - Kentec Medical, Inc - 2012-10-19 — classification: No Action Indicated (NAI), source: FDA, date: October 19, 2012
- FDA Inspection 636354 - Kentec Medical, Inc - 2009-12-16 — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2009
- FDA Inspection 636354 - Kentec Medical, Inc - 2009-12-16 — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2009

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