FDA Inspection 977569 - Aesculap Inc - July 13, 2016

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Record Details

This FDA Inspection record concerns Aesculap Inc, with an inspection on July 13, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aesculap Inc
Inspection Date: July 13, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b5de35be-5f1a-4130-98f7-b9d1eb1a17cf