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FDA Inspection 1041732 — Qiagen Sciences LLC

Qiagen Sciences LLC — FEI 3003572099

The FDA completed an inspection of Qiagen Sciences LLC on February 21, 2018 in Germantown, MD. 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
February 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Germantown, MD (United States)

Facility

Other inspections at this facility

  • 1146298 (VAI Fri Jul 16 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 995735 (VAI Mon Dec 19 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 958088 (OAI Fri Feb 05 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919610 (NAI Thu Mar 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 886551 (NAI Thu Jun 26 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources