Labverity
Facility profile

HP Halden Pharma AS

Testing & analysis · Drug product manufacturing · OSTFOLD NO-1788 · Norway

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
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.

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Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

May 10, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

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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 history7 inspection records

FDA inspection history

7 records, Nov 2009 – May 2023 · 0 NAI · 7 VAI · 0 OAI

DateClassProject areaCitationsFY
May 10, 2023VAIDrug Quality AssuranceYes2023
Sep 3, 2019VAIDrug Quality AssuranceYes2019
May 26, 2017VAIDrug Quality Assurance2017
Jun 26, 2015VAIDrug Quality Assurance2015
Dec 20, 2013VAIDrug Quality Assurance2014
Aug 23, 2012VAIDrug Quality Assurance2012
Nov 17, 2009VAIDrug Quality Assurance2010

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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