Home / Companies / Corden Pharma Chenove

Corden Pharma Chenove FDA Record

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

Corden Pharma Chenove has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Corden Pharma Chenove, the most recent on May 6, 2009.

What these totals cover: FDA records filed under the name "Corden Pharma Chenove".

Latest inspection: Feb 14, 2025 · VAI

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	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Corden Pharma Chenove'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	1	0	0	0	0
2024	0	0	0	0	0
2023	0	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	1	0	0	0	0
2018	0	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.

Reviewing Corden Pharma Chenove 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 Chenove 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

Corden Pharma Chenove FDA Warning Letters

1 warning letter on May 6, 2009.

Issued	Subject	Issuing office	Close-out letter
May 6, 2009

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

5 inspections from Nov 20, 2009 to Feb 14, 2025.

Date	Site	Product	Classification	FEI
Feb 14, 2025	Chenove, France	Drugs	Voluntary Action Indicated (VAI)	3002808295
Sep 13, 2019	Chenove, France	Drugs	Voluntary Action Indicated (VAI)	3002808295
Aug 26, 2016	Chenove, France	Drugs	No Action Indicated (NAI)	3002808295
Mar 14, 2014	Chenove, France	Drugs	Voluntary Action Indicated (VAI)	3002808295
Nov 20, 2009	Chenove, France	Drugs	Voluntary Action Indicated (VAI)	3002808295

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.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under Corden Pharma Chenove: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, May 6, 2009.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3002808295	Chenove, France	5	Feb 14, 2025

Corden Pharma Chenove and the FDA: common questions

Has Corden Pharma Chenove received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Corden Pharma Chenove. The most recent is dated May 6, 2009.

Has Corden Pharma Chenove received an FDA Form 483?

FDA has not published a Form 483 for "Corden Pharma Chenove" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Corden Pharma Chenove?

The most recent FDA inspection on file ended Feb 14, 2025 at Chenove, France and was classified VAI. FDA has 5 inspections of Corden Pharma Chenove on file.

Need more than this page shows? Ask about Corden Pharma Chenove 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.