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Catalent — Dartford

Dartford, United Kingdom · CDMO

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

Site facts

Company
Catalent
Name(s) in FDA data
Catalent Micron Technologies, Limited
FEI number(s)
3002807652 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Dartford, United Kingdom
Records matched
6 FDA inspections
Most recent FDA inspection in dataset
22 Jun 2022 — VAI

Capabilities (from the company's website)

  • Small molecule
    …al scales. Contact Us About This Site View Job Openings Facility at a Glance Service Area Small Molecule Facility Type Development Manufacturing Commercialization Certifications Highlights Regul…
  • Highly potent (HPAPI)
    …particle size reduction. It offers micronization, material characterization and handling highly potent compounds at both clinical and commercial scales. Contact Us About This Site View Job Ope…
  • Oral solid dose
    …ronization and Milling Small Molecule Commercialization Commercial CGMP Manufacturing for Oral Solid & Liquid Micronization and Milling Quality & Certifications Certifications ISO 14001 ISO…
  • Spray drying & particle engineering
    …on Hub Dartford Kent, United Kingdom Catalent’s Dartford facility serves as a key hub for particle engineering services, with expertise in particle size reduction. It offers micronization, material ch…
  • Analytical testing
    …rtford facility is a specialized center focused on particle size reduction and integrated analytical services for the pharmaceutical industry, supporting programs from early-stage development through…
  • Solid-state & particle characterization
    …artford facility serves as a key hub for particle engineering services, with expertise in particle size reduction. It offers micronization, material characterization and handling highly potent…

Taken from the company's web page for this site. Source: https://www.catalent.com/locations/dartford-united-kingdom, 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. 22 Jun 2022
    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 3002807652, inspection ID 1179292)

  2. 03 May 2017
    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 3002807652, inspection ID 1096811)

  3. 19 Jan 2017
    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 3002807652, inspection ID 1016422)

  4. 11 Apr 2014
    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 3002807652, inspection ID 877097)

  5. 25 Aug 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 3002807652, inspection ID 744909)

  6. 08 Apr 2009
    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 3002807652, inspection ID 575677)

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.