FDA Inspection
Kentec Medical, IncKentec Medical, Inc – FDA Inspection, Sep 24, 2014
Record Details
This FDA Inspection record concerns Kentec Medical, Inc, with an inspection on September 24, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kentec Medical, Inc
- Inspection Date
- September 24, 2014
- Product Type
- Devices
View Company Profile
ID · bd5ba38e-f756-41fa-a386-defecb57535c
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 897383
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Kentec Medical, Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 30, 2018 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 11, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 19, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 16, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Kentec Medical, Inc
- FDA Inspection 1060879 - 2018-07-30
- FDA Inspection 928285 - 2015-05-11
- FDA Inspection 803967 - 2012-10-19
- FDA Inspection 636354 - 2009-12-16
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