FDA Warning Letter — OPTILASA, S.L.

Case 129010 — FEI 3001022138

The FDA took a Warning Letter action against OPTILASA, S.L. on November 29, 2010 (Madrid, Spain). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
OPTILASA, S.L.
Date
November 29, 2010
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Madrid (Spain)