FDA Inspection 665884 — Abbott Vascular

Abbott Vascular — FEI 3005070406

The FDA completed an inspection of Abbott Vascular on May 27, 2010 in Menlo Park, 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
May 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Menlo Park, CA (United States)