FDA Inspection 1312482 — Qiagen Manchester Ltd.

Qiagen Manchester Ltd. — FEI 3009391812

The FDA completed an inspection of Qiagen Manchester Ltd. on February 24, 2026 in Manchester. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 24, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Manchester (United Kingdom)

Additional Details

Sponsor, Contract Research Organization