FDA Inspection 862326 — Lutonix Inc.

Lutonix Inc. — FEI 3006513822

The FDA completed an inspection of Lutonix Inc. on January 15, 2014 in Tempe, AZ. 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
January 15, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Tempe, AZ (United States)