FDA Inspection 919565 - PureTek Corporation - March 18, 2015
FDA Inspection 919565 for PureTek Corporation on March 18, 2015. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 919565 for PureTek Corporation on March 18, 2015. Classification: Voluntary Action Indicated (VAI).
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Company
PureTek CorporationInspection Date
March 18, 2015
Product Type
Cosmetics
ID: f3c1da5d-7a4d-424a-9a68-3495355ff7b9
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