FDA Inspection
Arthrex GmbhArthrex Gmbh – FDA Inspection, Oct 12, 2016
Record Details
This FDA Inspection record concerns Arthrex Gmbh, with an inspection on October 12, 2016, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Arthrex Gmbh
- Inspection Date
- October 12, 2016
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · fb10b72a-ad8d-4f44-9f80-b71d44be426e
Inspection Facts
- Inspection number
- 996312
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Arthrex Gmbh
3| Date | Classification | Office | Project area |
|---|---|---|---|
| October 31, 2018 | Not classified | Office of Inspections and Investigations | |
| October 9, 2017 | Not classified | Office of Inspections and Investigations | |
| September 27, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Arthrex Gmbh
- FDA Inspection 1106560 - 2018-10-31
- FDA Inspection 1045696 - 2017-10-09
- FDA Inspection 853020 - 2013-09-27
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