FDA Inspection 594199 — LCA Vision Inc.

LCA Vision Inc. — FEI 3007678698

The FDA completed an inspection of LCA Vision Inc. on Jul 1, 2009 in Rockville, MD. 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
Jul 1, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Rockville, MD (United States)