FDA Warning Letter — Optovue, Inc.

Case 104365 — FEI 3005950902

The FDA took a Warning Letter action against Optovue, Inc. on June 11, 2010 (Fremont, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Optovue, Inc.
Date
June 11, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Fremont, CA (United States)