FDA Inspection 899347 — Qiagen Manchester Ltd.

Qiagen Manchester Ltd. — FEI 3009391812

The FDA completed an inspection of Qiagen Manchester Ltd. on September 18, 2014 in Manchester. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 18, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Manchester (United Kingdom)

Additional Details

Postmarket Audit Inspections

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures