FDA Inspection 721626 — Abbott Vascular

Abbott Vascular — FEI 3004635528

The FDA completed an inspection of Abbott Vascular on April 20, 2011 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
April 20, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Santa Clara, CA (United States)

Additional Details

Sponsor, Contract Research Organization