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FDA Import Refusal BDG-0044603-2/21/1 — AKE INTERNATIONAL

AKE INTERNATIONAL — FEI 3013558148

The FDA refused shipment BDG-0044603-2/21/1 from AKE INTERNATIONAL (United Kingdom) on Aug 2, 2017. The refused product falls under Devices — EMERGENCY RESPONSE SAFETY KIT. Cited charges: 118,3280

Refusal details

Date
Aug 2, 2017
Country
United Kingdom
Product Category
Devices
Product Code
80OKI EMERGENCY RESPONSE SAFETY KIT
Charges
118,3280

FDA data resources

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