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Curia — Springfield

Springfield, Missouri, United States · CDMO

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

Site facts

Company
Curia
Name(s) in FDA data
Curia Missouri, Inc.
FEI number(s)
1941037 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Springfield, Missouri, United States 65807
Records matched
6 FDA inspections
Most recent FDA inspection in dataset
02 Dec 2025 — NAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …xperts An experienced technical and operations team focused on controlled and large-scale API manufacture. Reactor capacity 120 to 6,000 L A flexible reactor fleet spans development q…
  • Controlled substances
    …Skip to content Curia – Springfield, MO, USA Controlled substance manufacturing from gram to metric ton, with large-scale organometallic and cryogenic chem…

Taken from the company's web page for this site. Source: https://curiaglobal.com/facilities/springfield-mo/, 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. 02 Dec 2025
    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 1941037, inspection ID 1294960)

  2. 02 Aug 2019
    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 1941037, inspection ID 1101780)

  3. 09 Feb 2017
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 1941037, inspection ID 1009880)

  4. 08 Aug 2014
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 1941037, inspection ID 891078)

  5. 06 Jan 2012
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 1941037, inspection ID 762259)

  6. 22 Apr 2010
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 1941037, inspection ID 658410)

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.