# FDA Inspection 1206181 - Arthrex, Inc. - May 05, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/arthrex-inc/db41feaf-cb3c-46d0-8676-c2fc59ce221b
Source feed: FDA_Inspections

> FDA Inspection 1206181 for Arthrex, Inc. on May 05, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1206181
- Company Name: Arthrex, Inc.
- Inspection Date: 2023-05-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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