FDA Inspection 802483 - Propper Mfg Co Inc - October 03, 2012

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Record Details

This FDA Inspection record concerns Propper Mfg Co Inc, with an inspection on October 3, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Propper Mfg Co Inc
Inspection Date: October 3, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0f83a175-6cad-4063-a0c7-fe7d6663ef78

Violation Codes2

21 CFR 820.100(b)21 CFR 820.198(a)

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