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FDA Inspection 1029301 — Alexion Pharma LLC

Alexion Pharma LLC — FEI 3011263308

The FDA completed an inspection of Alexion Pharma LLC on October 19, 2017 in Bogart, GA. 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
October 19, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bogart, GA (United States)

Facility

Other inspections at this facility

  • 1223315 (NAI Thu Nov 16 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1113081 (NAI Wed Oct 23 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941833 (NAI Thu Aug 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941636 (VAI Mon Aug 10 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 927284 (NAI Wed Jan 14 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources