FDA Inspection 987720 - Aesculap AG - September 22, 2016

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Record Details

This FDA Inspection record concerns Aesculap AG, with an inspection on September 22, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aesculap AG
Inspection Date: September 22, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d8506a1b-1251-46d1-8992-ae661dece800