FDA Inspection 1025962 - Virtex - September 21, 2017

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Record Details

This FDA Inspection record concerns Virtex, with an inspection on September 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Virtex
Inspection Date: September 21, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ca2a8961-471a-44da-bc79-d0a621bf2df7

Violation Codes2

21 CFR 803.1721 CFR 820.72(a)

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