FDA Inspection 816142 — Abbott Vascular

Abbott Vascular — FEI 3006604866

The FDA completed an inspection of Abbott Vascular on January 16, 2013 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
January 16, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Temecula, CA (United States)

Additional Details

Postmarket Audit Inspections