FDA Import Refusal AEK-2139130-4/10002/1F — BIOPLUS CO LTD
The FDA refused shipment AEK-2139130-4/10002/1F from BIOPLUS CO LTD (South Korea) on Oct 2, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charges: 118,237,3280,336,84 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Oct 2, 2026
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
- Charges
- 118,237,3280,336,84