FDA Inspection 809812 - P-Ryton Corp - December 06, 2012

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Record Details

This FDA Inspection record concerns P-Ryton Corp, with an inspection on December 6, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: P-Ryton Corp
Inspection Date: December 6, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 834eaaea-b72f-4c57-a6ce-bf312853aa3a

Violation Codes5

21 CFR 820.100(a)21 CFR 820.18121 CFR 820.18421 CFR 820.20(c)21 CFR 820.80(a)

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