FDA Import Refusal 004-9970664-6/1/1 — Gvb Gelimed

Gvb Gelimed — FEI 3005037907

The FDA refused shipment 004-9970664-6/1/1 from Gvb Gelimed (Germany) on Jul 7, 2006. The refused product falls under Devices — ELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH. Cited charge: 341 This firm has 1 other import refusal on record.

Refusal details

Date
Jul 7, 2006
Country
Germany
Product Category
Devices
Product Code
89IKT ELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH
Charges
341

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