FDA Import Refusal AEK-1062474-7/6/1 — Kao Corporation

Kao Corporation — FEI 3002343252

The FDA refused shipment AEK-1062474-7/6/1 from Kao Corporation (Japan) on Aug 1, 2016. The refused product falls under Drugs and Biologics — ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Aug 1, 2016
Country
Japan
Product Category
Drugs and Biologics
Product Code
66PBO99 ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
Charges
118

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.