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Manufacturing facility

Eurofins Amatsi Analytics

A single plant registered with the FDA to make drugs for the US market. Below is where it is and the drugs whose FDA labels list this site as performing a manufacturing step — so if this plant has a problem, these are the products that could be affected.

Country
France
Registered address
Parc De Genibrat, Fontenilles, 31470, France (FRA)
Operations here
analysis
FDA identifiers
FEI 3006118993 · DUNS 270324185

FDA inspection history

Outcomes of closed FDA inspections at this site (drug and biologic program areas).

  • VAIBioresearch Monitoring2023-11-03
  • VAIDrug Quality Assurance2021-08-05
  • NAIDrug Quality Assurance2016-09-28
  • NAIDrug Quality Assurance2014-02-04

Drugs this plant is listed as making

2 distinct drugs across 2 products name this site in their FDA label.

Sources:the establishment's name, address, and country from FDA's Drug Establishments Current Registration Site (DECRS); the drug-to-facility links from DailyMed SPL drug labels, matched by the facility's DUNS number; inspection outcomes from the FDA Data Dashboard, matched by FEI; shortage status from FDA's drug shortage database. More on how this is built. Educational only.