FDA Import Refusal AEK-0046386-8/30003/1 — Novo Nordisk
The FDA refused shipment AEK-0046386-8/30003/1 from Novo Nordisk (India) on Mar 27, 2026. The refused product falls under Devices — INTRODUCER, SYRINGE NEEDLE. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Mar 27, 2026
- Country
- India
- Product Category
- Devices
- Product Code
- 80KZH INTRODUCER, SYRINGE NEEDLE
- Charges
- 118,3280