FDA Import Refusal AEK-1906171-9/1/1 — Gn Resound Gmbh

Gn Resound Gmbh — FEI 3004207128

The FDA refused shipment AEK-1906171-9/1/1 from Gn Resound Gmbh (Germany) on Apr 5, 2016. The refused product falls under Devices — NYSTAGMOGRAPH. Cited charge: 341

Refusal details

Date
Apr 5, 2016
Country
Germany
Product Category
Devices
Product Code
84GWN NYSTAGMOGRAPH
Charges
341

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