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Facility profile

Dipharma Francis Srl

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Milano 20021 · Italy

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed4 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

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)

Jul 15, 2022 · 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, May 2009 – Jul 2022 · 3 NAI · 4 VAI · 0 OAI

DateClassProject areaCitationsFY
Jul 15, 2022VAIDrug Quality Assurance2022
Sep 13, 2019NAIDrug Quality Assurance2019
Oct 25, 2018VAIDrug Quality Assurance2019
Mar 14, 2017VAIDrug Quality Assurance2017
May 6, 2015VAIDrug Quality Assurance2015
Jul 19, 2012NAIDrug Quality Assurance2012
May 15, 2009NAIDrug Quality Assurance2009

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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