FDA inspection

CardioFocus, Inc.: FDA inspection ending Jun 30, 2017

FDA inspection 1016613 · Voluntary Action Indicated (VAI) · Marlborough, MA

Key facts

Inspection ID 1016613
Firm CardioFocus, Inc.
FEI number 3001451473
Address 500 Nickerson Rd Ste 500-200
City Marlborough
State MA
ZIP 01752
Country United States
Fiscal year 2017
Inspection end date Jun 30, 2017
Classification Voluntary Action Indicated (VAI)
Project area Radiation Control and Health Safety Act
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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