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Curia — Boecillo

Boecillo, Spain · CDMO

This is a record of what regulators published, not a rating.

Site facts

Company
Curia
Name(s) in FDA data
Curia Spain SAU
FEI number(s)
3002996872 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Boecillo, Spain
Records matched
8 FDA inspections
Most recent FDA inspection in dataset
27 Feb 2023 — VAI

Capabilities (from the company's website)

  • Sterile fill-finish
    …op shop for steroid development through commercialization, with segregated facilities and aseptic processing purpose-built for this specialized product class. Particle size control 20+ years of p…
  • API / drug substance (chemical)
    …Skip to content Curia – Valladolid, Spain Steroids, hormones and sterile APIs, from development through commercialization on one campus. Curia’s Valladolid facility de…
  • Highly potent (HPAPI)
    …segregated steroid and hormone facilities, 20+ years of particle size control and OEB1-5 high-potency capability, inspected by the FDA, PMDA, the Spanish Agency and ANVISA. Facility at a glan…
  • Spray drying & particle engineering
    …sing purpose-built for this specialized product class. Particle size control 20+ years of particle engineering More than 20 years of experience in particle size control spans micronization, milling an…
  • Analytical testing
    …le size control spans micronization, milling and controlled crystallization, supported by analytical method development. API sterilization Aseptic filtration and crystallization under containment T…
  • Microbiology
    …chnology, with leading-edge control of particle size distribution, particulate matter and endotoxins. High potency OEB1-5 with isolator technology High-potency facilities span OEB1 through…
  • Solid-state & particle characterization
    …360 experts, Valladolid combines segregated steroid and hormone facilities, 20+ years of particle size control and OEB1-5 high-potency capability, inspected by the FDA, PMDA, the Spanish Agenc…

Taken from the company's web page for this site. Source: https://curiaglobal.com/facilities/valladolid-spain/, 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.

  1. 27 Feb 2023
    FDA 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 3002996872, inspection ID 1277041)

  2. 12 Mar 2020
    FDA 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 3002996872, inspection ID 1147255)

  3. 28 May 2018
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002996872, inspection ID 1059038)

  4. 21 Oct 2016
    FDA 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 3002996872, inspection ID 993118)

  5. 21 Mar 2014
    FDA 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 3002996872, inspection ID 873220)

  6. 23 Jun 2011
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002996872, inspection ID 734342)

  7. 17 Jun 2011
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002996872, inspection ID 734341)

  8. 27 Oct 2008
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002996872, inspection ID 549060)

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.