FDA Import Refusal FR1-0014943-9/1/1 — Cardionovum Gmbh

Cardionovum Gmbh — FEI 3010040929

The FDA refused shipment FR1-0014943-9/1/1 from Cardionovum Gmbh (Germany) on Mar 1, 2013. The refused product falls under Devices — CATHETER, RETENTION TYPE, BALLOON. Cited charges: 118,3741,508

Refusal details

Date
Mar 1, 2013
Country
Germany
Product Category
Devices
Product Code
78EZL CATHETER, RETENTION TYPE, BALLOON
Charges
118,3741,508

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