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Facility profile

Novo Nordisk A/S

Testing & analysis · Drug product manufacturing · Hovedstaden 2880 · Denmark

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed11 registered company locations
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

AnalysisActive pharmaceutical ingredient (API) manufactureManufacture
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Mar 29, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2012

More than five years old · review later records.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history10 inspection records

FDA inspection history

10 records, Mar 2009 – Mar 2023 · 5 NAI · 4 VAI · 1 OAI

DateClassProject areaCitationsFY
Mar 29, 2023VAIDrug Quality Assurance2023
Dec 5, 2019VAIDrug Quality Assurance2020
May 18, 2018NAIDrug Quality Assurance2018
May 18, 2018NAIBlood and Blood Products2018
Feb 8, 2017VAIBlood and Blood Products2017
Apr 8, 2016NAIDrug Quality Assurance2016
Sep 3, 2013VAIDrug Quality AssuranceYes2013
Mar 20, 2012OAIDrug Quality Assurance2012
May 13, 2009NAIBioresearch Monitoring2009
Mar 6, 2009NAIDrug Quality Assurance2009

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

Dec 12, 2012Warning Letter · CDER
Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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