FDA Inspection
Arthrex, Inc.Arthrex, Inc. – FDA Inspection, Oct 20, 2017
Record Details
This FDA Inspection record concerns Arthrex, Inc., with an inspection on October 20, 2017, issued by the Florida District Office, covering medical devices & rad health.
- Company
- Arthrex, Inc.
- Inspection Date
- October 20, 2017
- Product Type
- Medical Devices & Rad Health
- Office
- Florida District Office
View Company Profile
ID · 3527512d-3639-4b9c-a245-804da80662e4
Inspection Facts
- Inspection number
- 1051363
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Arthrex, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| January 13, 2025 | VAI | Florida District Office | Compliance: Medical Devices |
| May 5, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 30, 2018 | Not classified | Florida District Office | |
| August 25, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 30, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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