FDA Inspection 796781 - Aesculap Inc - August 30, 2012

FDA Inspection 796781 for Aesculap Inc on August 30, 2012. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 796781 for Aesculap Inc on August 30, 2012. Classification: No Action Indicated (NAI).

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Record Information

Company

Aesculap Inc

Inspection Date

August 30, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fda53588-dd8f-4730-b112-4a3ea4d5503a

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