FDA Import Refusal 799-0950326-4/1/1 — Acuregen

Acuregen — FEI 3010391997

The FDA refused shipment 799-0950326-4/1/1 from Acuregen (United Kingdom) on Oct 28, 2013. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charges: 118,341,508

Refusal details

Date
Oct 28, 2013
Country
United Kingdom
Product Category
Devices
Product Code
80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
Charges
118,341,508

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