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Curia — Aurangabad

Aurangabad, India · CDMO

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

Site facts

Company
Curia
Name(s) in FDA data
Curia India Private Limited
FEI number(s)
3008580576 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Aurangabad, India
Records matched
2 FDA inspections
Most recent FDA inspection in dataset
21 Jul 2026 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …Skip to content Curia – Aurangabad, India API and intermediate development and manufacturing, with more than 100,000 L of total reactor…
  • Spray drying & particle engineering
    …iving sponsors access to chemistry that many manufacturers avoid. Particle size reduction Micronization below 10 microns A state-of-the-art micronization facility reduces API particle size…
  • Solid-state & particle characterization
    …nge of chemistries. The site pairs specialized capabilities in thiophosgene chemistry and particle size reduction with multi-agency inspection history spanning the FDA, TGA and PMDA. Facility a…

Taken from the company's web page for this site. Source: https://curiaglobal.com/facilities/aurangabad-india/, 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. 21 Jul 2026
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). 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 3008580576, inspection ID 1330244)

  2. 16 Feb 2024
    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 3008580576, inspection ID 1233776)

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.