FDA Inspection 838673 - Sanofi Pasteur - June 21, 2013
FDA Inspection 838673 for Sanofi Pasteur on June 21, 2013. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 838673 for Sanofi Pasteur on June 21, 2013. Classification: Voluntary Action Indicated (VAI).
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Company
Sanofi PasteurInspection Date
June 21, 2013
Product Type
Biologics
ID: 1e03f767-3438-49e8-814a-069ddc9e9de8
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