FDA Inspection 899351 - Direx Systems Corp. - October 08, 2014

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Record Details

This FDA Inspection record concerns Direx Systems Corp., with an inspection on October 8, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Direx Systems Corp.
Inspection Date: October 8, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 28f333c4-6100-4b01-9fd7-e0507ce1a2b6

Violation Codes2

21 CFR 820.18421 CFR 820.20(c)

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