FDA Warning Letter — EEG Info

Case 296398 — FEI 3009138210

The FDA took a Warning Letter action against EEG Info on August 16, 2012 (Woodland Hills, CA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
EEG Info
Date
August 16, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Woodland Hills, CA (United States)