FDA Inspection 808977 — CardioFocus, Inc.

CardioFocus, Inc. — FEI 3001451473

The FDA completed an inspection of CardioFocus, Inc. on November 28, 2012 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
November 28, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Marlborough, MA (United States)

Additional Details

Sponsor, Contract Research Organization