FDA Import Refusal AEK-5096513-3/11/1K — Sungshim Medicare Co.,Ltd.
The FDA refused shipment AEK-5096513-3/11/1K from Sungshim Medicare Co.,Ltd. (South Korea) on Sep 12, 2018. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,3280 This firm has 1 other import refusal on record.
Refusal Details
- Date
- Sep 12, 2018
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
- Charges
- 118,3280