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Facility profile

Trifarma S.p.A.

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Rozzano · Italy

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed2 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) manufacture
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)

Sep 27, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2014

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 history6 inspection records

FDA inspection history

6 records, Jan 2010 – Sep 2024 · 1 NAI · 4 VAI · 1 OAI

DateClassProject areaCitationsFY
Sep 27, 2024VAIDrug Quality Assurance2024
Feb 28, 2019VAIDrug Quality Assurance2019
Jan 27, 2017VAIDrug Quality Assurance2017
Feb 27, 2015VAIDrug Quality Assurance2015
Jan 29, 2014OAIDrug Quality Assurance2014
Jan 28, 2010NAIDrug Quality Assurance2010

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

Matched compliance actions

Jul 7, 2014Warning 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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