FDA Inspection 841196 — PixxGen Corporation

PixxGen Corporation — FEI 3008164200

The FDA completed an inspection of PixxGen Corporation on June 26, 2013 in Anyang. 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
June 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Anyang (Korea (the Republic of))