FDA Inspection
EPflex Feinwerktechnik GmbHEPflex Feinwerktechnik GmbH – FDA Inspection, Feb 26, 2015
Record Details
This FDA Inspection record concerns EPflex Feinwerktechnik GmbH, with an inspection on February 26, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- EPflex Feinwerktechnik GmbH
- Inspection Date
- February 26, 2015
- Product Type
- Devices
View Company Profile
ID · c9fe4e65-afba-4b98-a507-1c7e29ef235f
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 921735
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of EPflex Feinwerktechnik GmbH
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 19, 2024 | NAI | Office of Inspections and Investigations | Postmarket Assurance: Medical Devices |
| June 13, 2013 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
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