FDA Import Refusal AEK-9633718-1/10002/1 — LEO Pharma Ireland

LEO Pharma Ireland — FEI 3002807468

The FDA refused shipment AEK-9633718-1/10002/1 from LEO Pharma Ireland (Ireland) on Aug 7, 2026. The refused product falls under Drugs and Biologics — BETAMETHASONE DIPROPIONATE (GLUCOCORTICOID). Cited charge: 75 This firm has 4 other import refusals on record.