FDA Inspection 772777 — EEG Info

EEG Info — FEI 3009138210

The FDA completed an inspection of EEG Info on March 19, 2012 in Woodland Hills, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 19, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Woodland Hills, CA (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
330921 CFR 820.120(b)Examination for accuracy