FDA Import Refusal 799-2260081-0/11/1 — VIANT AURA GMBH
The FDA refused shipment 799-2260081-0/11/1 from VIANT AURA GMBH (Germany) on Aug 9, 2019. The refused product falls under Devices — PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE. Cited charges: 118,3280,508
Refusal details
- Date
- Aug 9, 2019
- Country
- Germany
- Product Category
- Devices
- Product Code
- 74KFM PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE
- Charges
- 118,3280,508