FDA Inspection 605389 — Abbott Medical

Abbott Medical — FEI 2938836

The FDA completed an inspection of Abbott Medical on July 29, 2009 in Sunnyvale, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 29, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Sunnyvale, CA (United States)