FDA Inspection 586922 - Aesculap AG - June 05, 2009

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Record Details

This FDA Inspection record concerns Aesculap AG, with an inspection on June 5, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aesculap AG
Inspection Date: June 5, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c9190058-cfde-4729-8878-80a5b33ea71b