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
- Archimedesweg 25, Leiden, South Holland 2333 CM, Netherlands (NLD)
- Operations here
- analysis
- FDA identifiers
- FEI 3004939239 · DUNS 405855359
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2022-07-01
- VAIDrug Quality Assurance2019-05-01
- VAIDrug Quality Assurance2016-09-16
- VAIDrug Quality Assurance2013-03-18
Drugs this plant is listed as making
2 distinct drugs across 2 products name this site in their FDA label.
- MotixafortideBioLineRx USA Inc
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.