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Facility profile

Novo Nordisk A/S - Hax

Testing & analysis · Drug product manufacturing · Hovedstaden 2820 · 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) manufactureLabelManufacturePack
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)

Jun 1, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

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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 – Jun 2023 · 2 NAI · 8 VAI · 0 OAI

DateClassProject areaCitationsFY
Jun 1, 2023VAIDrug Quality Assurance2023
May 8, 2018NAIDrug Quality Assurance2018
Jun 14, 2016NAIDrug Quality Assurance2016
Nov 6, 2015VAIBlood and Blood Products2016
May 13, 2014VAIDrug Quality Assurance2014
May 1, 2013VAIBlood and Blood Products2013
Jun 26, 2012VAIDrug Quality Assurance2012
Feb 17, 2011VAIBlood and Blood Products2011
Mar 6, 2009VAIDrug Quality Assurance2009
Mar 5, 2009VAIHuman Cellular, Tissue, and Gene Therapies2009

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

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

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

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