FDA Import Refusal AEK-9586082-7/1/1 — Gambro Do Brasil Ltda
The FDA refused shipment AEK-9586082-7/1/1 from Gambro Do Brasil Ltda (Brazil) on Sep 12, 2008. The refused product falls under Devices — AUTOMATED BLOOD CELL AND PLASMA SEPARATOR FOR THERAPEUTIC PURPOSES, CENTRIFUGE. Cited charge: 341
Refusal details
- Date
- Sep 12, 2008
- Country
- Brazil
- Product Category
- Devices
- Product Code
- 78LKN AUTOMATED BLOOD CELL AND PLASMA SEPARATOR FOR THERAPEUTIC PURPOSES, CENTRIFUGE
- Charges
- 341