Home / Companies / Corden Pharma S.P.A.

Corden Pharma S.P.A.

FDA Regulatory Profile

Corden Pharma S.P.A. has 0 FDA recalls, 13 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Corden Pharma S.P.A." and its spelling variant "Corden Pharma".

Latest inspection: Oct 15, 2025 · VAI

Reviewing Corden Pharma S.P.A. 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 Corden Pharma S.P.A. 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	13	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Corden Pharma S.P.A.'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	2	0	0	0	0
2024	0	0	0	0	0
2023	0	0	0	0	0
2022	2	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	1	0	0	0	0
2018	2	0	0	0	0
2017	0	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

13 inspections from Jul 16, 2009 to Oct 15, 2025.

Date	Site	Product	Classification	FEI
Oct 15, 2025	Plankstadt, Germany	Drugs	Voluntary Action Indicated (VAI)	3007014398
Mar 28, 2025	Caponago, Italy	Drugs	Voluntary Action Indicated (VAI)	3002880938
Dec 2, 2022	Caponago, Italy	Drugs	Voluntary Action Indicated (VAI)	3002880938
Sep 14, 2022	Plankstadt, Germany	Drugs	Voluntary Action Indicated (VAI)	3007014398
Jun 14, 2019	Caponago, Italy	Drugs	Voluntary Action Indicated (VAI)	3002880938
Jul 10, 2018	Caponago, Italy	Veterinary	Voluntary Action Indicated (VAI)	3002880938
Jul 6, 2018	Plankstadt, Germany	Drugs	No Action Indicated (NAI)	3007014398
Jul 15, 2016	Caponago, Italy	Veterinary	Voluntary Action Indicated (VAI)	3002880938
Oct 24, 2014	Plankstadt, Germany	Drugs	No Action Indicated (NAI)	3007014398
Mar 14, 2014	Caponago, Italy	Drugs	Voluntary Action Indicated (VAI)	3002880938
Oct 28, 2011	Caponago, Italy	Drugs	Voluntary Action Indicated (VAI)	3002880938
Nov 17, 2009	Plankstadt, Germany	Drugs	No Action Indicated (NAI)	3007014398
Jul 16, 2009	Caponago, Italy	Drugs	Voluntary Action Indicated (VAI)	3002880938

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

2 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3007014398	Plankstadt, Germany	5	Oct 15, 2025
FEI 3002880938	Caponago, Italy	8	Mar 28, 2025

Need more than this page shows? Ask about Corden Pharma S.P.A. 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.