FDA WARNING_LETTER - Peter Schiff Enterprises - April 12, 2013

FDA WARNING_LETTER for Peter Schiff Enterprises on April 12, 2013. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Peter Schiff Enterprises on April 12, 2013. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.22

21 CFR 820.80(d)

21 U.S.C. 360j(f)(2)

21 CFR 820.100(a)

21 CFR 820

21 CFR 820.20(c)

21 U.S.C. 351(h)

21 U.S.C. 360j(f)(1)

21 U.S.C. 321(h)(2)

21 CFR 820.40

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Record Information

Company

Peter Schiff Enterprises

Inspection Date

April 12, 2013

Product Type

Devices

Office

New Orleans District Office

People

Patricia K. Schafer

ID: 68d7f3bd-bbcf-4a8e-9b63-c958fef436f1

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