FDA Inspection 696082 - Propper Mfg Co Inc - October 27, 2010

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Record Details

This FDA Inspection record concerns Propper Mfg Co Inc, with an inspection on October 27, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Propper Mfg Co Inc
Inspection Date: October 27, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 04094c7f-a34e-430a-9b38-c1b2a559e190

Violation Codes4

21 CFR 803.17(a)(3)21 CFR 820.100(b)21 CFR 820.80(b)21 CFR 820.90(b)(2)

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