FDA Warning Letter — EyeKon Medical, Inc.

Case 42979 — FEI 1038833

The FDA took a Warning Letter action against EyeKon Medical, Inc. on December 9, 2008 (Clearwater, FL). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
EyeKon Medical, Inc.
Date
December 9, 2008
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Clearwater, FL (United States)