FDA Device Entity Profile: NOVO NORDISK INC.

Known Identifiers & Locations

FEI Numbers 2244771, 3002807751, 3003131673, 3004547341, 3005186124

Owner Operator Numbers 9027307

Locations Covered HILLEROED Hovedstaden, DK; HJOERRING Nordjylland, DK; Kalundborg Sjalland, DK; Plainsboro, NJ, US; Tianjin, CN

Registered Establishments (5)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
2244771	NOVO NORDISK INC.	Plainsboro, NJ, US	Complaint File Establishment per 21 CFR 820.198	View Details
3002807751	NOVO NORDISK A/S	Kalundborg Sjalland, DK	Manufacture Medical Device	View Details
3005186124	Novo Nordisk (China) Pharmaceuticals, Co. Ltd.	Tianjin, CN	Manufacture Medical Device	View Details
9681821	NOVO NORDISK A/S	HILLEROED Hovedstaden, DK	Develop Specifications But Do Not Manufacture At This Facility	View Details
9681822	NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI	HJOERRING Nordjylland, DK	Manufacture Medical Device	View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

AvaSpecs compiles public data records from the FDA database. This compiled profile does not indicate endorsement, safety, clearance, approval, or compliance status. AvaSpecs is a private search index and is not affiliated with the FDA or any government agency.