FDA Import Refusal AEK-2816010-6/11/1 — VIVATEC CO LTD
The FDA refused shipment AEK-2816010-6/11/1 from VIVATEC CO LTD (Japan) on Jan 9, 2017. The refused product falls under Devices — TOOTHBRUSH, MANUAL. Cited charges: 118,341
Refusal details
- Date
- Jan 9, 2017
- Country
- Japan
- Product Category
- Devices
- Product Code
- 76EFW TOOTHBRUSH, MANUAL
- Charges
- 118,341