FDA Inspection 551121 - VitalDyne, Inc - December 11, 2008

FDA Inspection 551121 for VitalDyne, Inc on December 11, 2008. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 551121 for VitalDyne, Inc on December 11, 2008. Classification: No Action Indicated (NAI).

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Record Information

Company

VitalDyne, Inc

Inspection Date

December 11, 2008

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8640cd0-c17c-4d38-9519-1bf2fd457a55

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