FDA Import Refusal AEK-3621937-3/11/1 — DreamCon Co. Ltd.
The FDA refused shipment AEK-3621937-3/11/1 from DreamCon Co. Ltd. (South Korea) on Jul 19, 2017. The refused product falls under Devices — LENS, CONTACT (OTHER MATERIAL) - DAILY. Cited charge: 508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Jul 19, 2017
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 86HQD LENS, CONTACT (OTHER MATERIAL) - DAILY
- Charges
- 508