FDA Inspection 818811 — K S Choi Corp

K S Choi Corp — FEI 1000519961

The FDA completed an inspection of K S Choi Corp on February 7, 2013 in Los Angeles, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
February 7, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Los Angeles, CA (United States)