FDA Inspection
QIAGEN Instruments AGQIAGEN Instruments AG – FDA Inspection, Oct 16, 2014
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
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ID · bebf1297-9b70-47f9-9c1c-20bffec409c7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 899915
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.22Quality Audits - defined intervals
Full citation text and observation details available on the Dashboard.
Other FDA inspections of QIAGEN Instruments AG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 14, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 19, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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