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FDA Inspection 1017182 — Abbott Laboratories

Abbott Laboratories — FEI 2919069

The FDA completed an inspection of Abbott Laboratories on May 17, 2017 in Santa Clara, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 17, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Clara, CA (United States)

Facility

Other inspections at this facility

  • 986276 (VAI Wed Aug 10 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 834101 (NAI Thu May 16 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 716720 (VAI Fri Apr 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 605426 (NAI Wed Aug 12 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources