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FDA Inspection 938440 — Alexion Pharmaceuticals, Inc.

Alexion Pharmaceuticals, Inc. — FEI 3006568549

The FDA completed an inspection of Alexion Pharmaceuticals, Inc. on August 12, 2015 in Smithfield, RI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 12, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Smithfield, RI (United States)

Facility

Other inspections at this facility

  • 1019062 (VAI Fri Jul 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 984855 (VAI Wed Aug 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 892913 (VAI Fri Aug 22 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 710477 (VAI Fri Feb 18 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources