FDA Warning Letter — Alcon LenSx, Inc.

Case 353122 — FEI 3008772169

The FDA took a Warning Letter action against Alcon LenSx, Inc. on December 3, 2012 (Aliso Viejo, CA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Alcon LenSx, Inc.
Date
December 3, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Aliso Viejo, CA (United States)