FDA Inspection 816389 — Abbott Vascular

Abbott Vascular — FEI 3004635528

The FDA completed an inspection of Abbott Vascular on February 8, 2013 in Santa Clara, 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 8, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Clara, CA (United States)