FDA Inspection 755405 — Abbott Vascular, Inc.

Abbott Vascular, Inc. — FEI 3000718335

The FDA completed an inspection of Abbott Vascular, Inc. on Dec 1, 2011 in Redwood City, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 1, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Redwood City, CA (United States)

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