FDA Inspection 672698 — Cardionics, Inc

Cardionics, Inc — FEI 1629623

The FDA completed an inspection of Cardionics, Inc on July 23, 2010 in Webster, TX. 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
July 23, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Webster, TX (United States)