FDA Import Refusal 1FX-8058282-8/10002/2 — MEDISEPTE E&C
The FDA refused shipment 1FX-8058282-8/10002/2 from MEDISEPTE E&C (South Korea) on Oct 9, 2026. The refused product falls under Devices — ACID, HYALURONIC, INTRAARTICULAR. Cited charge: 508 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Oct 9, 2026
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 87MOZ ACID, HYALURONIC, INTRAARTICULAR
- Charges
- 508