FDA Import Refusal 799-0844506-4/11/1 — Novo Nordisk A/S

Novo Nordisk A/S — FEI 3004547341

The FDA refused shipment 799-0844506-4/11/1 from Novo Nordisk A/S (Denmark) on Jun 26, 2017. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 341 This firm has 5 or more other import refusals on record.