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FDA Inspection 1012920 — Abbott Laboratories

Abbott Laboratories — FEI 1415939

The FDA completed an inspection of Abbott Laboratories on February 2, 2017 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 2, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
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))
  • 936765 (VAI Tue Aug 11 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 868086 (NAI Fri Feb 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources