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Manufacturing facility

Eurofins BioPharma Product Testing Hamburg GmbH

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
Germany
Registered address
Am Neuländer Gewerbepark 2, Hamburg, D-21079, Germany (DEU)
Operations here
analysis
FDA identifiers
FEI 3010166293 · DUNS 341475834

FDA inspection history

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

  • VAIDrug Quality Assurance2022-10-19
  • NAIDrug Quality Assurance2019-09-18
  • NAIDrug Quality Assurance2013-07-10

Drugs this plant is listed as making

1 distinct drugs across 1 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.