FDA Inspection 841575 - Aesculap AG - July 04, 2013

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Record Details

This FDA Inspection record concerns Aesculap AG, with an inspection on July 4, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aesculap AG
Inspection Date: July 4, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 79309850-27ab-496f-b74a-eecd0c9bc716