FDA Inspection
VertiFlex, Inc.FDA Inspection 993550 - VertiFlex, Inc. - July 19, 2016
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Record Details
This FDA Inspection record concerns VertiFlex, Inc., with an inspection on July 19, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 6108d677-efd7-463c-9701-55da1a8c017b
Violation Codes1
21 CFR 820.184
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