FDA inspection

Abbott Vascular: FDA inspection ending Feb 8, 2013

FDA inspection 816389 · No Action Indicated (NAI) · Santa Clara, CA

Key facts

Inspection ID 816389
Firm Abbott Vascular
FEI number 3004635528
Address 3200 Lakeside Dr
City Santa Clara
State CA
ZIP 95054
Country United States
Fiscal year 2013
Inspection end date Feb 8, 2013
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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