FDA Inspection
ARTHREX GMBHARTHREX GMBH – FDA Inspection, Oct 12, 2017
Record Details
This FDA Inspection record concerns ARTHREX GMBH, with an inspection on October 12, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- ARTHREX GMBH
- Inspection Date
- October 12, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 6dd80c30-8f6c-454d-97e8-e64b04b88eda
Inspection Facts
- Inspection number
- 1045707
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of ARTHREX GMBH
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 13, 2016 | Not classified | Office of Inspections and Investigations | |
| September 25, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for ARTHREX GMBH
- FDA Inspection 993948 - 2016-10-13
- FDA Inspection 853087 - 2013-09-25
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