FDA Inspection 755405 — Abbott Vascular, Inc.

Abbott Vascular, Inc. — FEI 3000718335

The FDA completed an inspection of Abbott Vascular, Inc. on December 1, 2011 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
December 1, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Redwood City, CA (United States)