FDA Inspection 869546 — Abbott Vascular

Abbott Vascular — FEI 3006604866

The FDA completed an inspection of Abbott Vascular on February 19, 2014 in Temecula, 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
February 19, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Temecula, CA (United States)