FDA Inspection 853010 — Qiagen Manchester Ltd.
The FDA completed an inspection of Qiagen Manchester Ltd. on September 12, 2013 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
- September 12, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Manchester (United Kingdom)
Additional Details
Postmarket Audit Inspections