FDA Inspection 1161220 - Artivion, Inc - January 20, 2022

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Record Details

This FDA Inspection record concerns Artivion, Inc, with an inspection on January 20, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company: Artivion, Inc
Inspection Date: January 20, 2022
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 27127e6f-da06-4a38-95c3-824e1e923ebd