# Qiagen Manchester Ltd., Manchester, United Kingdom – FDA Inspections

Source: https://www.keypedia.com/companies/qiagen-manchester-ltd/e5b42beb-90af-40a0-b5c7-a13071d026d9

> Inspection records and compliance data for Qiagen Manchester Ltd. in Manchester. 6 FDA inspections on record, 1 Form 483, last inspected February 24, 2026.

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## Details

- Name: Qiagen Manchester Ltd.
- FEI Number: 3009391812
- Address Line 1: St. Marys Hospital, Citylabs 2.0; Hathersage Road
- City: Manchester
- Country Name: United Kingdom
- Address: St. Marys Hospital, Citylabs 2.0; Hathersage Road, Manchester, United Kingdom
- Country: United Kingdom

## Related Documents

- FDA Inspection 1312482 - Qiagen Manchester Ltd. - 2026-02-24 — source: FDA, date: February 24, 2026
- FDA Inspection 1199453 - Qiagen Manchester Ltd. - 2022-11-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 10, 2022
- FDA Inspection 1117588 - Qiagen Manchester Ltd. - 2020-01-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2020
- [FDA Inspection 1043524 - Qiagen Manchester Ltd. - 2017-09-08](https://www.keypedia.com/records/fda_inspections/qiagen-manchester-ltd/b5bde329-0360-488f-9974-2375352f9662) — source: FDA, date: September 8, 2017
- FDA Inspection 899347 - Qiagen Manchester Ltd. - 2014-09-18 — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2014
- FDA Inspection 899347 - Qiagen Manchester Ltd. - 2014-09-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 18, 2014
- [FDA Inspection 899347 - Qiagen Manchester Ltd. - 2014-09-18](https://www.keypedia.com/records/fda_inspections/qiagen-manchester-ltd/ea003599-43a0-446a-bb5a-36cab48cde32) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2014
- FDA Inspection 853010 - Qiagen Manchester Ltd. - 2013-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2013
- FDA Inspection 853010 - Qiagen Manchester Ltd. - 2013-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2013

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