FDA Inspection 986649 - Aesculap Inc - September 14, 2016

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Record Details

This FDA Inspection record concerns Aesculap Inc, with an inspection on September 14, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aesculap Inc
Inspection Date: September 14, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4b635ce7-8c7f-4165-98bd-53399fc1b387