FDA Inspection 868672 - Veridiam, Inc. - March 06, 2014

FDA Inspection 868672 for Veridiam, Inc. on March 06, 2014. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 868672 for Veridiam, Inc. on March 06, 2014. Classification: No Action Indicated (NAI).

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Record Information

Company

Veridiam, Inc.

Inspection Date

March 6, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbcb07b9-3848-4175-8a19-da1384e99810

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