FDA Import Refusal AEK-0399730-0/10002/1 — Interojo Inc.
The FDA refused shipment AEK-0399730-0/10002/1 from Interojo Inc. (South Korea) on Jul 2, 2026. The refused product falls under Devices — LENSES, SOFT CONTACT, DAILY WEAR. Cited charge: 341 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Jul 2, 2026
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 86LPL LENSES, SOFT CONTACT, DAILY WEAR
- Charges
- 341