FDA Inspection 823538 - Virtex - March 26, 2013

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Record Details

This FDA Inspection record concerns Virtex, with an inspection on March 26, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Virtex
Inspection Date: March 26, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e1ff9294-d76e-4ca4-85e6-c0e5033c80dd

Violation Codes4

21 CFR 820.70(a)21 CFR 820.75(a)21 CFR 820.90(a)21 CFR 820.90(b)(2)

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