FDA Device Establishments · JSON-LD · Markdown

NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI

FEI 3004547341 · Manufacture Medical Device · Status: Active

FEI Number3004547341
Owner / OperatorNOVO NORDISK INC. (#9027307)
AddressSTENAGER ALLE 4, HJOERRING Nordjylland, --, DK
Mandatory US AgentNOVO NORDISK INC.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FMI
Regulation § (21 CFR)880.5570
Proprietary namesNOVOFINE 32G Tip

External sources

Source: openFDA. Public-domain (CC0).