FDA Inspection 954371 - Cardiox Corporation - December 18, 2015

FDA Inspection 954371 for Cardiox Corporation on December 18, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 954371 for Cardiox Corporation on December 18, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Cardiox Corporation

Inspection Date

December 18, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbdbbc38-d47f-4f1c-a5fc-8df25191946f

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