FDA Import Refusal AEK-3461489-8/11/1 — MEDIKOMP GMBH
The FDA refused shipment AEK-3461489-8/11/1 from MEDIKOMP GMBH (Germany) on Jul 12, 2017. The refused product falls under Devices — PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE. Cited charge: 3280
Refusal details
- Date
- Jul 12, 2017
- Country
- Germany
- Product Category
- Devices
- Product Code
- 74KFM PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE
- Charges
- 3280