FDA Inspection
Qiagen Manchester Ltd.Qiagen Manchester Ltd. – FDA Inspection, Sep 8, 2017
Record Details
This FDA Inspection record concerns Qiagen Manchester Ltd., with an inspection on September 8, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Qiagen Manchester Ltd.
- Inspection Date
- September 8, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · b5bde329-0360-488f-9974-2375352f9662
Inspection Facts
- Inspection number
- 1043524
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
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 18, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| 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 899347 - 2014-09-18
- FDA Inspection 853010 - 2013-09-12
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