Dipharma Francis S.R.L. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Dipharma Francis S.R.L. has 0 FDA recalls, 19 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Dipharma Francis S.R.L." is on file.

What these totals cover: FDA records filed under the name "Dipharma Francis S.R.L." and its spelling variant "Dipharma Francis".

Latest inspection
Sep 13, 2024 · VAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections19Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Dipharma Francis S.R.L.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Dipharma Francis S.R.L.: FDA inspections per year 2017: 2 inspections220172018: 3 inspections320182019: 2 inspections220192020: 0 inspections020202021: 0 inspections020212022: 3 inspections320222023: 0 inspections020232024: 1 inspections120242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
202300000
202230000
202100000
202000000
201920000
201830000
201720000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Reviewing Dipharma Francis S.R.L. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Dipharma Francis S.R.L. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Recent FDA inspections

19 inspections from May 15, 2009 to Sep 13, 2024.

DateSiteProductClassificationFEI
Sep 13, 2024Mereto Di Tomba, ItalyDrugsVoluntary Action Indicated (VAI)3002806810
Sep 2, 2022Caronno Pertusella, ItalyDrugsVoluntary Action Indicated (VAI)3003270894
Jul 15, 2022Baranzate, ItalyDrugsVoluntary Action Indicated (VAI)3001624853
Feb 25, 2022Mereto Di Tomba, ItalyDrugsVoluntary Action Indicated (VAI)3002806810
Sep 13, 2019Baranzate, ItalyDrugsNo Action Indicated (NAI)3001624853
Feb 8, 2019Caronno Pertusella, ItalyDrugsVoluntary Action Indicated (VAI)3003270894
Oct 25, 2018Baranzate, ItalyDrugsVoluntary Action Indicated (VAI)3001624853
Apr 20, 2018Mereto Di Tomba, ItalyDrugsVoluntary Action Indicated (VAI)3002806810
Feb 23, 2018Caronno Pertusella, ItalyDrugsVoluntary Action Indicated (VAI)3003270894
Apr 28, 2017Mereto Di Tomba, ItalyDrugsVoluntary Action Indicated (VAI)3002806810
Mar 14, 2017Baranzate, ItalyDrugsVoluntary Action Indicated (VAI)3001624853
Feb 11, 2016Caronno Pertusella, ItalyDrugsVoluntary Action Indicated (VAI)3003270894
May 6, 2015Baranzate, ItalyDrugsVoluntary Action Indicated (VAI)3001624853
Mar 7, 2014Mereto Di Tomba, ItalyDrugsVoluntary Action Indicated (VAI)3002806810
Nov 23, 2012Caronno Pertusella, ItalyDrugsVoluntary Action Indicated (VAI)3003270894
Jul 19, 2012Baranzate, ItalyDrugsNo Action Indicated (NAI)3001624853
Dec 20, 2010Mereto Di Tomba, ItalyDrugsNo Action Indicated (NAI)3002806810
Feb 11, 2010Caronno Pertusella, ItalyDrugsVoluntary Action Indicated (VAI)3003270894
May 15, 2009Baranzate, ItalyDrugsNo Action Indicated (NAI)3001624853
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

3 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3002806810Mereto Di Tomba, Italy6Sep 13, 2024
FEI 3003270894Caronno Pertusella, Italy6Sep 2, 2022
FEI 3001624853Baranzate, Italy7Jul 15, 2022

Dipharma Francis S.R.L. and the FDA: common questions

Has Dipharma Francis S.R.L. received an FDA warning letter?

No FDA warning letter addressed to the name "Dipharma Francis S.R.L." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Dipharma Francis S.R.L. received an FDA Form 483?

FDA has not published a Form 483 for "Dipharma Francis S.R.L." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Dipharma Francis S.R.L.?

The most recent FDA inspection on file ended Sep 13, 2024 at Mereto Di Tomba, Italy and was classified VAI. FDA has 19 inspections of Dipharma Francis S.R.L. on file.

Need more than this page shows? Ask about Dipharma Francis S.R.L. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

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