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

Record Details

This FDA Inspection record concerns Arthrex, Inc., with an inspection on May 5, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: Arthrex, Inc.
Inspection Date: May 5, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · db41feaf-cb3c-46d0-8676-c2fc59ce221b

Violation Codes2

21 CFR 803.1721 CFR 820.198(a)

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