FDA Inspection 1314374 — Qiagen GmbH

Qiagen GmbH — FEI 3004013603

The FDA completed an inspection of Qiagen GmbH on March 12, 2026 in Hilden. 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
March 12, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Hilden (Germany)