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FDA Inspection 721939 — St. Jude Medical

St. Jude Medical — FEI 2182269

The FDA completed an inspection of St. Jude Medical on April 21, 2011 in Minnetonka, MN. 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
April 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)

Facility

Other inspections at this facility

  • 1089439 (NAI Wed Mar 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 967750 (NAI Mon Apr 11 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 903706 (NAI Thu Jul 31 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 771571 (NAI Tue Feb 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 712895 (NAI Tue Mar 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources