Home / Companies / Delpharm Milano Srl

Delpharm Milano Srl FDA Record

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

Delpharm Milano Srl has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Delpharm Milano Srl" is on file.

What these totals cover: FDA records filed under the name "Delpharm Milano Srl" and its spelling variant "Delpharm Milano".

Latest inspection: Feb 18, 2022 · VAI

Reviewing Delpharm Milano Srl 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 Delpharm Milano Srl 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

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

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	5	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Delpharm Milano Srl's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	0	0	0	0	0
2024	0	0	0	0	0
2023	0	0	0	0	0
2022	1	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	0	0	0	0	0
2018	0	0	0	0	0
2017	1	0	0	0	0

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.

Recent FDA inspections

5 inspections from Jun 24, 2011 to Feb 18, 2022.

Date	Site	Product	Classification	FEI
Feb 18, 2022	Segrate, Italy	Drugs	Voluntary Action Indicated (VAI)	3003716872
May 12, 2017	Segrate, Italy	Drugs	Voluntary Action Indicated (VAI)	3003716872
Sep 25, 2015	Segrate, Italy	Drugs	Voluntary Action Indicated (VAI)	3003716872
Sep 19, 2013	Segrate, Italy	Drugs	Voluntary Action Indicated (VAI)	3003716872
Jun 24, 2011	Segrate, Italy	Drugs	No Action Indicated (NAI)	3003716872

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

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3003716872	Segrate, Italy	5	Feb 18, 2022

Delpharm Milano Srl and the FDA: common questions

Has Delpharm Milano Srl received an FDA warning letter?

No FDA warning letter addressed to the name "Delpharm Milano Srl" 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 Delpharm Milano Srl received an FDA Form 483?

FDA has not published a Form 483 for "Delpharm Milano Srl" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Delpharm Milano Srl?

The most recent FDA inspection on file ended Feb 18, 2022 at Segrate, Italy and was classified VAI. FDA has 5 inspections of Delpharm Milano Srl on file.

Need more than this page shows? Ask about Delpharm Milano Srl 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.