FDA Inspection 1015191 - FlexDex Inc. - June 22, 2017

FDA Inspection 1015191 for FlexDex Inc. on June 22, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1015191 for FlexDex Inc. on June 22, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

FlexDex Inc.

Inspection Date

June 22, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff515bac-4e9f-40c0-aec8-80e05a76ac5a

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