FDA Inspection 938243 — Abbott Vascular, Inc.

Abbott Vascular, Inc. — FEI 3000718335

The FDA completed an inspection of Abbott Vascular, Inc. on August 14, 2015 in Redwood City, 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
August 14, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Redwood City, CA (United States)