FDA inspection

Abbott Vascular: FDA inspection ending Sep 23, 2005

FDA inspection 397331 · No Action Indicated (NAI) · Menlo Park, CA

Key facts

Inspection ID 397331
Firm Abbott Vascular
FEI number 3005070406
Address 3885 Bohannon Dr
City Menlo Park
State CA
ZIP 94025-1001
Fiscal year 2005
Inspection end date Sep 23, 2005
Classification No Action Indicated (NAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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