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FDA Import Refusal 799-7481002-8/11/1 — Occlutech GmbH

Occlutech GmbH — FEI 3014616394

The FDA refused shipment 799-7481002-8/11/1 from Occlutech GmbH (Germany) on Jun 29, 2020. The refused product falls under Devices — DEVICE, TRANSCATHETER CARDIAC OCCLUSION. Cited charges: 118,3280

Refusal details

Date
Jun 29, 2020
Country
Germany
Product Category
Devices
Product Code
74MLV DEVICE, TRANSCATHETER CARDIAC OCCLUSION
Charges
118,3280

FDA data resources

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