FDA Inspection 1080023 - DRE Medical Group Inc - February 21, 2019

FDA Inspection 1080023 for DRE Medical Group Inc on February 21, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1080023 for DRE Medical Group Inc on February 21, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

DRE Medical Group Inc

Inspection Date

February 21, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fcfb99f6-2971-4fd1-a845-ac8deb466401

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