# FDA Inspection 621663 - Arthrex, Inc. - October 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/arthrex-inc/69b01e82-4598-4d2f-9f4b-284f2dbb8b4d
Source feed: FDA_Inspections

> FDA Inspection 621663 for Arthrex, Inc. on October 09, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 621663
- Company Name: Arthrex, Inc.
- Inspection Date: 2009-10-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1256990 - 2025-01-13](https://www.keypedia.com/records/fda_inspections/arthrex-inc/c1ab486b-3e07-429a-9db2-0a4512da02dc)
- [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)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7