# QIAGEN Instruments AG – FDA Inspection, Jul 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/qiagen-instruments-ag/93a66d7c-b404-4d58-ad46-1ff0a5eeb0c7
Source feed: FDA_Inspections

> FDA inspection 843989 of QIAGEN Instruments AG, July 19, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 843989
- Company Name: QIAGEN Instruments AG
- Inspection Date: 2013-07-19
- 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: 4

## 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 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