FDA Inspection 899915 - QIAGEN Instruments AG - October 16, 2014

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Record Details

This FDA Inspection record concerns QIAGEN Instruments AG, with an inspection on October 16, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: QIAGEN Instruments AG
Inspection Date: October 16, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · bebf1297-9b70-47f9-9c1c-20bffec409c7

Violation Codes1

21 CFR 820.22

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