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Manufacturing facility

Eurofins BioPharma Product Testing Leiden B.V.

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
Netherlands
Registered address
Darwinweg 24, Leiden, South Holland 2333 CR, Netherlands (NLD)
Operations here
analysis
FDA identifiers
FEI 3004594563 · DUNS 490477955

FDA inspection history

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

  • VAIDrug Quality Assurance2022-07-01
  • VAIDrug Quality Assurance2019-08-21
  • VAIDrug Quality Assurance2017-09-07
  • VAIDrug Quality Assurance2014-11-06
  • VAIDrug Quality Assurance2011-09-15

Drugs this plant is listed as making

1 distinct drugs across 7 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.