FDA Inspection 818828 - PAJUNK GMBH MEDIZINTECHNOLOGIE - January 31, 2013

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Record Details

This FDA Inspection record concerns PAJUNK GMBH MEDIZINTECHNOLOGIE, with an inspection on January 31, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: PAJUNK GMBH MEDIZINTECHNOLOGIE
Inspection Date: January 31, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 19b45a19-26b9-4952-9e95-4a7e3499e3a6

Violation Codes5

21 CFR 803.17(a)(1)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.70(c)

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