FDA Inspection
Qiagen Manchester Ltd.Qiagen Manchester Ltd. – FDA Inspection, Sep 18, 2014
Record Details
This FDA Inspection record concerns Qiagen Manchester Ltd., with an inspection on September 18, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Qiagen Manchester Ltd.
- Inspection Date
- September 18, 2014
- Product Type
- Devices
View Company Profile
ID · ea003599-43a0-446a-bb5a-36cab48cde32
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 899347
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Qiagen Manchester Ltd.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 24, 2026 | Not classified | Office of Inspections and Investigations | |
| November 10, 2022 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| January 24, 2020 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 8, 2017 | Not classified | Office of Inspections and Investigations | |
| September 12, 2013 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Qiagen Manchester Ltd.
- FDA Inspection 1312482 - 2026-02-24
- FDA Inspection 1199453 - 2022-11-10
- FDA Inspection 1117588 - 2020-01-24
- FDA Inspection 1043524 - 2017-09-08
- FDA Inspection 853010 - 2013-09-12
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