Establishment registration
NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI
FDA establishment registration 9681822 · HJOERRING Nordjylland, DK
Key facts
| Registration number | 9681822 |
|---|---|
| Establishment name | NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI |
| Owner/operator | NOVO NORDISK INC. |
| Owner/operator number | 9027307 |
| FEI number | 3004547341 |
| Address | STENAGER ALLE 4 |
| City | HJOERRING Nordjylland |
| Country | DK |
| Registration valid through | 2026 |
| Product codes listed | FMI |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database