FDA Import Refusal AEK-0899186-0/30002/1 — Across Co., Ltd
The FDA refused shipment AEK-0899186-0/30002/1 from Across Co., Ltd (South Korea) on Aug 14, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charge: 237 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Aug 14, 2026
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
- Charges
- 237