FDA Inspection 1035639 - Propper Mfg Co Inc - December 21, 2017

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Record Details

This FDA Inspection record concerns Propper Mfg Co Inc, with an inspection on December 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Propper Mfg Co Inc
Inspection Date: December 21, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · bcef571b-c9dd-4072-86f4-fc70d970192f

Violation Codes5

21 CFR 820.100(b)21 CFR 820.70(c)21 CFR 820.72(a)21 CFR 820.75(a)21 CFR 820.86

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