FDA Import Refusal AEK-3877717-0/11/1 — MEDI DIRECT INTL
The FDA refused shipment AEK-3877717-0/11/1 from MEDI DIRECT INTL (United Kingdom) on Oct 25, 2017. The refused product falls under Devices — STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF. Cited charges: 118,3280,341,508
Refusal details
- Date
- Oct 25, 2017
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 84GZJ STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF
- Charges
- 118,3280,341,508