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FDA Inspection
•QIAGEN Instruments AG•October 16, 2014

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

Full citation text and observation details available on the Dashboard.

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