FDA Inspection 993550 - VertiFlex, Inc. - July 19, 2016

FDA Inspection 993550 for VertiFlex, Inc. on July 19, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 993550 for VertiFlex, Inc. on July 19, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.184

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Record Information

Company

VertiFlex, Inc.

Inspection Date

July 19, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fdf35d7a-fc36-4ed2-bc7e-506b38c4d27a

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