FDA Inspection 625448 - Advanced OrthoPro, Inc. - November 09, 2009
FDA Inspection 625448 for Advanced OrthoPro, Inc. on November 09, 2009. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 625448 for Advanced OrthoPro, Inc. on November 09, 2009. Classification: Voluntary Action Indicated (VAI).
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Company
Advanced OrthoPro, Inc.Inspection Date
November 9, 2009
Product Type
Devices
ID: 112466b2-0c97-4301-9fa8-558f06b5f071
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