FDA Inspection
Arthrex, Inc.Arthrex, Inc. – FDA Inspection, Nov 30, 2018
Record Details
This FDA Inspection record concerns Arthrex, Inc., with an inspection on November 30, 2018, issued by the Florida District Office, covering medical devices & rad health.
- Company
- Arthrex, Inc.
- Inspection Date
- November 30, 2018
- Product Type
- Medical Devices & Rad Health
- Office
- Florida District Office
View Company Profile
ID · 026fb82f-14a3-4eb4-9bba-28de8b04a0d8
Inspection Facts
- Inspection number
- 1101957
- 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 |
| October 20, 2017 | 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 |
Other documents for Arthrex, Inc.
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.