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Dipharma Francis Srl FDA Inspection Record

FEI 3002806810 · Inspections, Form 483s, warning letters and import refusals

Dipharma Francis Srl is an FDA-registered facility (FEI 3002806810) located in Udine, IT. Registered operations: ANALYSIS; API MANUFACTURE. RegDataLab tracks 6 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Sep 13, 2024: Voluntary Action Indicated (VAI)
Inspections on record
6 (5 VAI, 1 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Sep 13, 2024Voluntary Action Indicated (VAI)No citations listed
Feb 25, 2022Voluntary Action Indicated (VAI)No citations listed
Apr 20, 2018Voluntary Action Indicated (VAI)No citations listed
Apr 28, 2017Voluntary Action Indicated (VAI)No citations listed
Mar 7, 2014Voluntary Action Indicated (VAI)No citations listed
Dec 20, 2010No Action Indicated (NAI)No citations listed

FDA record score

9 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

5 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAISep 13, 20246 x 0.63.6
Inspection classified VAIFeb 25, 20226 x 0.63.6
Inspection classified VAIApr 20, 20186 x 0.251.5
Inspection classified VAIApr 28, 2017Only the 3 most recent VAI inspections add points0
Inspection classified VAIMar 7, 201410 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Dipharma Francis Srl
Location
Udine (IT)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; API MANUFACTURE
Source
decrs

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.