Home / Companies / Eurofins Amatsi Analytics

Eurofins Amatsi Analytics

FDA Regulatory Profile

Eurofins Amatsi Analytics has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Eurofins Amatsi Analytics".

Latest inspection
May 20, 2026 · VAI

Reviewing Eurofins Amatsi Analytics 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 Eurofins Amatsi Analytics 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
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections8Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

Eurofins Amatsi Analytics: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 1 inspections120192020: 0 inspections020202021: 1 inspections120212022: 0 inspections020222023: 2 inspections220232024: 0 inspections020242025: 0 inspections020252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202500000
202400000
202320000
202200000
202110000
202000000
201910000
201800000
201700000

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

8 inspections from Oct 8, 2010 to May 20, 2026.

DateSiteProductClassificationFEI
May 20, 2026Fontenilles, FranceDrugsVoluntary Action Indicated (VAI)3006118993
Dec 21, 2023Peyruis, FranceDrugsVoluntary Action Indicated (VAI)3012886212
Nov 3, 2023Fontenilles, FranceDrugsVoluntary Action Indicated (VAI)3006118993
Aug 5, 2021Fontenilles, FranceDrugsVoluntary Action Indicated (VAI)3006118993
Mar 15, 2019Peyruis, FranceDrugsVoluntary Action Indicated (VAI)3012886212
Sep 28, 2016Fontenilles, FranceDrugsNo Action Indicated (NAI)3006118993
Feb 4, 2014Fontenilles, FranceDrugsNo Action Indicated (NAI)3006118993
Oct 8, 2010Fontenilles, FranceVeterinaryNo Action Indicated (NAI)3006118993
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.

FacilityLocationInspectionsLatest
FEI 3006118993Fontenilles, France6May 20, 2026
FEI 3012886212Peyruis, France2Dec 21, 2023

Need more than this page shows? Ask about Eurofins Amatsi Analytics 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.

FDA data resources

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