FDA Inspection 803984 — Abbott Medical

Abbott Medical — FEI 2017865

The FDA completed an inspection of Abbott Medical on October 17, 2012 in Sylmar, 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
October 17, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Sylmar, CA (United States)