Fareva Pau FDA Record

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

Fareva Pau has 0 FDA recalls, 10 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Fareva Pau, the most recent on Mar 26, 2010.

What these totals cover: FDA records filed under the name "Fareva Pau".

Latest inspection
Jan 17, 2025 · 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
Inspections10Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

Fareva Pau: FDA inspections per year 2017: 1 inspections120172018: 1 inspections120182019: 0 inspections020192020: 0 inspections020202021: 1 inspections120212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 1 inspections120252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202510000
202400000
202300000
202200000
202110000
202000000
201900000
201810000
201710000

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.

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Fareva Pau FDA Warning Letters

1 warning letter on Mar 26, 2010.

IssuedSubjectIssuing officeClose-out letter
Mar 26, 2010

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

10 inspections from Sep 8, 2009 to Jan 17, 2025.

DateSiteProductClassificationFEI
Jan 17, 2025Idron, FranceDrugsVoluntary Action Indicated (VAI)3002806390
Nov 5, 2021Idron, FranceDrugsVoluntary Action Indicated (VAI)3002806390
Apr 27, 2018Idron, FranceDrugsVoluntary Action Indicated (VAI)3002806390
Apr 13, 2017Idron, FranceDrugsNo Action Indicated (NAI)3002806390
Jun 10, 2015Idron, FranceDrugsVoluntary Action Indicated (VAI)3002806390
Feb 26, 2013Idron, FranceDrugsVoluntary Action Indicated (VAI)3002806390
May 12, 2011Idron, FranceDrugsNo Action Indicated (NAI)3002806390
May 12, 2011Idron, FranceDrugsVoluntary Action Indicated (VAI)3002806390
Sep 8, 2009Idron, FranceDrugsOfficial Action Indicated (OAI)3002806390
Sep 8, 2009Idron, FranceDrugsOfficial Action Indicated (OAI)3002806390
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 Fareva Pau: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Mar 26, 2010.

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.

FacilityLocationInspectionsLatest
FEI 3002806390Idron, France10Jan 17, 2025

Fareva Pau and the FDA: common questions

Has Fareva Pau received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Fareva Pau. The most recent is dated Mar 26, 2010.

Has Fareva Pau received an FDA Form 483?

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

When did the FDA last inspect Fareva Pau?

The most recent FDA inspection on file ended Jan 17, 2025 at Idron, France and was classified VAI. FDA has 10 inspections of Fareva Pau on file, 2 of them classified OAI (official action indicated).

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