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FDA Inspection 928695 — CardioFocus, Inc.

CardioFocus, Inc. — FEI 3001451473

The FDA completed an inspection of CardioFocus, Inc. on May 7, 2015 in Marlborough, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 7, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Marlborough, MA (United States)

Facility

Other inspections at this facility

  • 1177544 (VAI Thu Aug 11 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1016613 (VAI Fri Jun 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 808977 (NAI Wed Nov 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 746966 (NAI Fri Sep 23 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources