FDA Inspection 1116761 - PureTek Corporation - January 30, 2020
FDA Inspection 1116761 for PureTek Corporation on January 30, 2020. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 1116761 for PureTek Corporation on January 30, 2020. Classification: Voluntary Action Indicated (VAI).
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Company
PureTek CorporationInspection Date
January 30, 2020
Product Type
Drugs
ID: 6bfc016f-d6d9-4703-b6b3-519218c7507f
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