FDA Inspection 825133 - Peter Schiff Enterprises - April 12, 2013

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Record Details

This FDA Inspection record concerns Peter Schiff Enterprises, with an inspection on April 12, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Peter Schiff Enterprises
Inspection Date: April 12, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9bf7597e-6c28-4954-8320-19fb55025451

Violation Codes5

21 CFR 820.100(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.4021 CFR 820.80(d)

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