Labverity
Facility profile

Latina Pharma S.P.A

Testing & analysis · Drug product manufacturing · Latina 04013 · Italy

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.

AnalysisActive pharmaceutical ingredient (API) manufactureLabelManufacturePack
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)

Jan 19, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2016

More than five years old · review later records.

Understand this record

Use the evidence, then ask for fit.

Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

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

Ask next

Ask what was corrected and review any later inspection or follow-up record.

Method and source details
View full inspection and compliance history5 inspection records

FDA inspection history

5 records, Jul 2013 – Jan 2024 · 0 NAI · 4 VAI · 1 OAI

DateClassProject areaCitationsFY
Jan 19, 2024VAIDrug Quality Assurance2024
Sep 27, 2019VAIDrug Quality Assurance2019
Apr 21, 2017VAIDrug Quality Assurance2017
May 29, 2015OAIDrug Quality Assurance2015
Jul 24, 2013VAIDrug Quality Assurance2013

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

Matched compliance actions

May 20, 2016Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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

Ask about services