# FDA Inspection 843989 - QIAGEN Instruments AG - July 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/67ef7bc9-a552-4a85-967c-3fd1d830d849
Source feed: FDA_Inspections

> FDA Inspection 843989 for QIAGEN Instruments AG on July 19, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 843989
- Company Name: QIAGEN Instruments AG
- Inspection Date: 2013-07-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 957347 - 2016-01-14](https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/cbf79113-0a26-49b1-9193-4f69c69c0d1b)
- [FDA Inspection 957347 - 2016-01-14](https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/fb56f140-968a-47ce-af45-61586cd7e946)
- [FDA Inspection 957347 - 2016-01-14](https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/7dd7e943-5104-479b-b396-d1d8974a5f87)
- [FDA Inspection 899915 - 2014-10-16](https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/8e3464c2-b8dc-4b3b-8be4-822b06ba4534)
- [FDA Inspection 899915 - 2014-10-16](https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/bebf1297-9b70-47f9-9c1c-20bffec409c7)

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