FDA Inspection
Arthrex, Inc.FDA Inspection 1206181 - Arthrex, Inc. - May 05, 2023
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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.
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ID · db41feaf-cb3c-46d0-8676-c2fc59ce221b
Violation Codes2
21 CFR 803.1721 CFR 820.198(a)
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