FDA Import Refusal AEK-1806363-4/11/1 — LETINAR CO LTD
The FDA refused shipment AEK-1806363-4/11/1 from LETINAR CO LTD (South Korea) on Oct 4, 2022. The refused product falls under Devices — LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION). Cited charge: 3280
Refusal details
- Date
- Oct 4, 2022
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 86HQG LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
- Charges
- 3280