FDA Import Refusal 799-5858930-0/21/1 — NOVO NORDISK

NOVO NORDISK — FEI 3014158939

The FDA refused shipment 799-5858930-0/21/1 from NOVO NORDISK (Canada) on Dec 19, 2021. The refused product falls under Devices — NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE. Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 19, 2021
Country
Canada
Product Category
Devices
Product Code
79GAA NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE
Charges
75

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.