FDA Import Refusal AEK-0116211-3/10002/1 — Novo Nordisk A/S

Novo Nordisk A/S — FEI 3000151819

The FDA refused shipment AEK-0116211-3/10002/1 from Novo Nordisk A/S (Denmark) on Apr 10, 2026. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,3260,3280,508 This firm has 5 or more other import refusals on record.