FDA Inspection 587052 — LCA Vision Inc.

LCA Vision Inc. — FEI 3007625186

The FDA completed an inspection of LCA Vision Inc. on May 29, 2009 in Edina, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 29, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Edina, MN (United States)