FDA Inspection 961641 - LANXESS Corporation - January 15, 2016
FDA Inspection 961641 for LANXESS Corporation on January 15, 2016. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 961641 for LANXESS Corporation on January 15, 2016. Classification: Voluntary Action Indicated (VAI).
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Company
LANXESS CorporationInspection Date
January 15, 2016
Product Type
Drugs
ID: 1ee869f3-9bf9-4e73-907a-50e428024ad8
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