FDA Inspection 735962 - LCA Vision, Inc dba LasikPlus - July 25, 2011
FDA Inspection 735962 for LCA Vision, Inc dba LasikPlus on July 25, 2011. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 735962 for LCA Vision, Inc dba LasikPlus on July 25, 2011. Classification: Voluntary Action Indicated (VAI).
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Inspection Date
July 25, 2011
Product Type
Devices
ID: fc61a73f-c77b-4c88-bd2d-8c0106aecf7a
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