FDA Inspection 1178394 - Aesculap AG - July 21, 2022

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Record Details

This FDA Inspection record concerns Aesculap AG, with an inspection on July 21, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aesculap AG
Inspection Date: July 21, 2022
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c301202a-fd12-4f51-912f-3075d36b9ada