FDA Inspection 761092 - Aurident Inc - December 07, 2011

FDA Inspection 761092 for Aurident Inc on December 07, 2011. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 761092 for Aurident Inc on December 07, 2011. Classification: No Action Indicated (NAI).

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Record Information

Company

Aurident Inc

Inspection Date

December 7, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9e69607-b00e-4efa-a22c-9569dc77e579

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