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FDA Inspection 802031 — Abbott Medical

Abbott Medical — FEI 2938836

The FDA completed an inspection of Abbott Medical on September 28, 2012 in Sunnyvale, 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
September 28, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)

Facility

Other inspections at this facility

  • 967466 (NAI Fri Jan 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 696712 (NAI Wed Nov 03 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 605389 (OAI Wed Jul 29 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources