FDA Inspection 816138 — EEG Info

EEG Info — FEI 3009138210

The FDA completed an inspection of EEG Info on January 30, 2013 in Woodland Hills, CA. 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 30, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Woodland Hills, CA (United States)