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EUROAPI — Frankfurt Am Main
Frankfurt Am Main, Germany · CDMO
Site facts
- Company
- EUROAPI
- Name(s) in FDA data
- EUROAPI Germany GmbH
- FEI number(s)
- 3020754015 (present in FDA Data Dashboard records for this name and city)
- Location (as in FDA data)
- Frankfurt Am Main, Germany
- Records matched
- 1 FDA inspection
- Most recent FDA inspection in dataset
- 04 Mar 2022 — VAI
Capabilities (from the company's website)
- Lyophilization
…des Organic synthesis (large-volume) GMP micronization (incl. cryomilling) Flow chemistry Lyophilisation…
- API / drug substance (chemical)
…Frankfurt | Germany API PRODUCING & DEVELOPMENT CENTER (CHEMISTRY+TIDES) 25+ APIs 110+ Customers served 50 countr…
- Peptides & oligonucleotides
…ations Key technologies & capabilities Multipurpose chemical site Solid phase chemistry : Peptides & Oligonucleotides Organic synthesis (large-volume) GMP micronization (incl. cryomilling)…
- Spray drying & particle engineering
…Solid phase chemistry : Peptides & Oligonucleotides Organic synthesis (large-volume) GMP micronization (incl. cryomilling) Flow chemistry Lyophilisation…
Taken from the part of the company's network/locations page that describes this site. Source: https://www.euroapi.com/en/industrial-footprint, checked 16 Oct 2026. Quoted text shows the wording each tag is based on.
Regulatory timeline
Newest first. Each entry links to the published source. Inspection classifications: NAI = no action indicated, VAI = voluntary action indicated, OAI = official action indicated (FDA definitions). Posted 483 citations are FDA's short summaries, not the full Form 483.
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04 Mar 2022FDA inspection FDA inspection classified VAI
Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.
Source: FDA Data Dashboard – Inspections (FEI 3020754015, inspection ID 1231135)
This is a record of what regulators published, not a rating. Absence of a record here does not mean no record exists; see methodology for what we check and how records are matched.