FDA Inspection 598757 - Artivion, Inc - May 01, 2009

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Record Details

This FDA Inspection record concerns Artivion, Inc, with an inspection on May 1, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Artivion, Inc
Inspection Date: May 1, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a5e12279-95d9-4329-96b5-7f9349600c49