FDA Inspection 1117588 — Qiagen Manchester Ltd.
The FDA completed an inspection of Qiagen Manchester Ltd. on January 24, 2020 in Manchester. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- January 24, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Manchester (United Kingdom)
Additional Details
Sponsor, Contract Research Organization