FDA Inspection 1049722 - Interpore Cross International, LLC - April 18, 2018
FDA Inspection 1049722 for Interpore Cross International, LLC on April 18, 2018. Classification: No Action Indicated (NAI).
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FDA Inspection 1049722 for Interpore Cross International, LLC on April 18, 2018. Classification: No Action Indicated (NAI).
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Inspection Date
April 18, 2018
Product Type
Biologics
ID: fd0c020a-e7b2-4a38-b360-e3949ce9f12a
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