FDA Inspection 559939 - ARP Manufacturing, LLC - January 28, 2009

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Record Details

This FDA Inspection record concerns ARP Manufacturing, LLC, with an inspection on January 28, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: ARP Manufacturing, LLC
Inspection Date: January 28, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 46ea76b1-448c-430b-9e1a-50961b991b7c

Violation Codes3

21 CFR 803.50(a)(1)21 CFR 820.198(c)21 CFR 820.22

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