FDA Import Refusal 112-0219556-2/1/1 — Suturex & Renodex S.A.
The FDA refused shipment 112-0219556-2/1/1 from Suturex & Renodex S.A. (France) on Jun 9, 2014. The refused product falls under Devices — STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF. Cited charges: 118,508
Refusal details
- Date
- Jun 9, 2014
- Country
- France
- Product Category
- Devices
- Product Code
- 84LGW STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
- Charges
- 118,508