FDA Inspection 1314374 — Qiagen GmbH

Qiagen GmbH — FEI 3004013603

The FDA completed an inspection of Qiagen GmbH on Mar 12, 2026 in Hilden. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Mar 12, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Hilden (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.