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Facility profile

Novartis Pharma AG

Testing & analysis · Drug product manufacturing · Basel · Switzerland

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed20 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

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)

Aug 30, 2022 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2011

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 history9 inspection records

FDA inspection history

9 records, Nov 2008 – Aug 2022 · 4 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Aug 30, 2022VAIDrug Quality Assurance2022
Jul 12, 2019NAIDrug Quality Assurance2019
Jul 6, 2017VAIDrug Quality Assurance2017
Jan 14, 2015NAIDrug Quality Assurance2015
Dec 5, 2013NAIDrug Quality Assurance2014
Jul 26, 2012VAIDrug Quality Assurance2012
Jul 18, 2012NAIDrug Quality Assurance2012
Nov 21, 2008VAIDrug Quality Assurance2009
Nov 6, 2008VAIBioresearch Monitoring2009

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

Matched compliance actions

Nov 18, 2011Warning 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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