FDA Inspection 853020 - Arthrex Gmbh - September 27, 2013

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Record Details

This FDA Inspection record concerns Arthrex Gmbh, with an inspection on September 27, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Arthrex Gmbh
Inspection Date: September 27, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 51f5c1f4-fea7-4e96-b366-eb9de394e0f7