Home / Inspections / 552672

FDA Inspection 552672 — Abbott Laboratories

Abbott Laboratories — FEI 1451914

The FDA completed an inspection of Abbott Laboratories on November 14, 2008 in North Chicago, 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
November 14, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
North Chicago, IL (United States)

Facility

Other inspections at this facility

  • 1090280 (NAI Wed Mar 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 796961 (VAI Fri Aug 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 715413 (VAI Thu Mar 10 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 675926 (NAI Tue Jul 27 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources