FDA Inspection
Kulzer, LLC.Kulzer, LLC. – FDA Inspection, Jul 12, 2017
Record Details
This FDA Inspection record concerns Kulzer, LLC., with an inspection on July 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 75779385-9f03-48a4-b562-03f7805082d9
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1024387
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Kulzer, LLC.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 12, 2018 | Not classified | Detroit District Office | |
| June 20, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 28, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 23, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kulzer, LLC.
- FDA Inspection 1120156 - 2018-10-12
- FDA Inspection 883853 - 2014-06-20
- FDA Inspection 747015 - 2011-09-28
- FDA Inspection 589433 - 2009-06-23
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