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FDA Inspection 736882 — Abbott Laboratories

Abbott Laboratories — FEI 1415939

The FDA completed an inspection of Abbott Laboratories on July 29, 2011 in Abbott Park, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 29, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Abbott Park, IL (United States)

Facility

Other inspections at this facility

  • 1229076 (NAI Wed May 29 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1084371 (VAI Fri Mar 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1024377 (NAI Fri May 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1012920 (VAI Thu Feb 02 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 936765 (VAI Tue Aug 11 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources