FDA Inspection 668303 — Abbott Vascular

Abbott Vascular — FEI 3005070406

The FDA completed an inspection of Abbott Vascular on June 3, 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
June 3, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Menlo Park, CA (United States)

Additional Details

Sponsor, Contract Research Organization