FDA Import Refusal AEK-0799505-0/1/1 — Vupiesse Italia Srl

Vupiesse Italia Srl — FEI 3004629141

The FDA refused shipment AEK-0799505-0/1/1 from Vupiesse Italia Srl (Italy) on Apr 27, 2015. The refused product falls under Devices — STIMULATOR, MUSCLE, POWERED, FOR MUSCLE CONDITIONING. Cited charge: 341 This firm has 3 other import refusals on record.

Refusal details

Date
Apr 27, 2015
Country
Italy
Product Category
Devices
Product Code
89NGX STIMULATOR, MUSCLE, POWERED, FOR MUSCLE CONDITIONING
Charges
341

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