FDA Inspection 894663 - Nexus Dx, Inc - September 09, 2014

FDA Inspection 894663 for Nexus Dx, Inc on September 09, 2014. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 894663 for Nexus Dx, Inc on September 09, 2014. Classification: No Action Indicated (NAI).

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Record Information

Company

Nexus Dx, Inc

Inspection Date

September 9, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: faf68961-0269-4795-96bf-bf3578dfc88c

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