FDA Import Refusal AEK-0317039-2/1/1 — Actreg (U.K.) Ltd.

Actreg (U.K.) Ltd. — FEI 3006482880

The FDA refused shipment AEK-0317039-2/1/1 from Actreg (U.K.) Ltd. (United Kingdom) on Dec 18, 2012. The refused product falls under Devices — COMPUTERS AND SOFTWARE, MEDICAL. Cited charges: 118,341 This firm has 1 other import refusal on record.

Refusal details

Date
Dec 18, 2012
Country
United Kingdom
Product Category
Devices
Product Code
80LNX COMPUTERS AND SOFTWARE, MEDICAL
Charges
118,341

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