FDA Inspection 638178 - Seiki, Inc. - December 01, 2009
FDA Inspection 638178 for Seiki, Inc. on December 01, 2009. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 638178 for Seiki, Inc. on December 01, 2009. Classification: Voluntary Action Indicated (VAI).
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Company
Seiki, Inc.Inspection Date
December 1, 2009
Product Type
Cosmetics
ID: fdabdf08-6add-401f-b508-0dff1d89d90f
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