# FDA Inspection 1256990 - Arthrex, Inc. - January 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/arthrex-inc/c1ab486b-3e07-429a-9db2-0a4512da02dc
Source feed: FDA_Inspections

> FDA Inspection 1256990 for Arthrex, Inc. on January 13, 2025. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1256990
- Company Name: Arthrex, Inc.
- Inspection Date: 2025-01-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Florida District Office

## Related Documents

- [FDA Inspection 1256990 - 2025-01-13](https://www.keypedia.com/records/fda_inspections/arthrex-inc/07abdf4d-2fb6-4fde-914d-39f6d9cd6c51)
- [FDA Inspection 1206181 - 2023-05-05](https://www.keypedia.com/records/fda_inspections/arthrex-inc/db41feaf-cb3c-46d0-8676-c2fc59ce221b)
- [FDA Inspection 1206181 - 2023-05-05](https://www.keypedia.com/records/fda_inspections/arthrex-inc/84399818-3db6-4312-85c7-53a31ae5e1ff)
- [FDA Inspection 984081 - 2016-08-25](https://www.keypedia.com/records/fda_inspections/arthrex-inc/b6873f18-9cbc-4440-954b-1a550f6f9bd0)
- [FDA Inspection 984081 - 2016-08-25](https://www.keypedia.com/records/fda_inspections/arthrex-inc/c8a55436-e787-4a35-8a73-f6ce301c51d3)

Company: https://www.keypedia.com/companies/arthrex-inc/e18abb8a-3bf8-462d-b279-f969cd710c14

Office: https://www.keypedia.com/offices/florida-district-office/95b2a118-0b78-46e0-a54c-982bd7ce51c9