# Kentec Medical, Inc – FDA Inspection, Sep 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/bd5ba38e-f756-41fa-a386-defecb57535c
Source feed: FDA_Inspections

> FDA inspection 897383 of Kentec Medical, Inc, September 24, 2014. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897383
- Company Name: Kentec Medical, Inc
- Inspection Date: 2014-09-24
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1060879 - 2018-07-30](https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/53a53752-8517-4022-8a6e-43817f29509a)
- FDA Inspection 928285 - 2015-05-11
- FDA Inspection 803967 - 2012-10-19
- FDA Inspection 636354 - 2009-12-16

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7