FDA Inspection
Nugyn, IncNugyn, Inc – FDA Inspection, Aug 2, 2017
Record Details
This FDA Inspection record concerns Nugyn, Inc, with an inspection on August 2, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Marissa S. Steinhagen (Issuing Officer)
View Company Profile
ID · 693da43f-6f8c-434a-8151-15abe2f26815
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1020397
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Nugyn, Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 28, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 1, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Nugyn, Inc
- FDA Inspection 838407 - 2013-06-28
- FDA Inspection 683435 - 2010-09-01
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