# QIAGEN Instruments AG – FDA Inspection, Oct 16, 2014

Source: https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/bebf1297-9b70-47f9-9c1c-20bffec409c7
Source feed: FDA_Inspections

> FDA inspection 899915 of QIAGEN Instruments AG, October 16, 2014. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 899915
- Company Name: QIAGEN Instruments AG
- Inspection Date: 2014-10-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 957347 - 2016-01-14](https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/fb56f140-968a-47ce-af45-61586cd7e946)
- [FDA Inspection 843989 - 2013-07-19](https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/93a66d7c-b404-4d58-ad46-1ff0a5eeb0c7)

Company: https://www.keypedia.com/companies/qiagen-instruments-ag/a40c761e-d171-4981-ad0c-56b7d649af24

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7