FDA Inspection 1043580 - Vidatak LLC - February 02, 2018

FDA Inspection 1043580 for Vidatak LLC on February 02, 2018. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1043580 for Vidatak LLC on February 02, 2018. Classification: No Action Indicated (NAI).

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Record Information

Company

Vidatak LLC

Inspection Date

February 2, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa4f0db0-a2b5-4977-b239-9e2bbc757324

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