Home / Inspections / 715413

FDA Inspection 715413 — Abbott Laboratories

Abbott Laboratories — FEI 1451914

The FDA completed an inspection of Abbott Laboratories on March 10, 2011 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
March 10, 2011
Fiscal Year
2011
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))
  • 675926 (NAI Tue Jul 27 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 552672 (VAI Fri Nov 14 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources