FDA Inspection 1008504 - Peter Schiff Enterprises - April 13, 2017

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Record Details

This FDA Inspection record concerns Peter Schiff Enterprises, with an inspection on April 13, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Peter Schiff Enterprises
Inspection Date: April 13, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 306ca0bc-b2b1-42b9-9947-dd9ad2ed9734

Violation Codes8

21 CFR 820.100(a)21 CFR 820.120(b)21 CFR 820.18421 CFR 820.20(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.40(a)21 CFR 820.75(a)

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