FDA Inspection 1029760 - DT MedTech, LLC - October 24, 2017

FDA Inspection 1029760 for DT MedTech, LLC on October 24, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1029760 for DT MedTech, LLC on October 24, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

DT MedTech, LLC

Inspection Date

October 24, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb9f2a0f-4dd2-4bf0-80c1-ecdb41584381

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