FDA Warning Letter — LCA Vision Inc.

Case 79172 — FEI 3007625186

The FDA took a Warning Letter action against LCA Vision Inc. on Oct 9, 2009 (Edina, MN). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
LCA Vision Inc.
Date
Oct 9, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Edina, MN (United States)