FDA inspection

Medtronic Ablation Frontiers: FDA inspection ending May 16, 2011

FDA inspection 727034 · Voluntary Action Indicated (VAI) · Carlsbad, CA

Key facts

Inspection ID 727034
Firm Medtronic Ablation Frontiers
FEI number 3007798852
Address 2210 Faraday Ave Ste 100
City Carlsbad
State CA
ZIP 92008
Country United States
Fiscal year 2011
Inspection end date May 16, 2011
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 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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