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Kindeva Drug Delivery — Loughborough

Loughborough, United Kingdom · CDMO

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

Site facts

Company
Kindeva Drug Delivery
Name(s) in FDA data
Kindeva Drug Delivery Limited
FEI number(s)
3002807586 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Loughborough, United Kingdom
Records matched
8 FDA inspections
Most recent FDA inspection in dataset
14 Mar 2025 — VAI

Capabilities (from the company's website)

  • Inhalation & nasal
    …analytical method development and validation and stability chambers with 24/7 monitoring. Inhalation expertise pMDI pressure and cold filling, pilot-scale filling with a variety of prop…
  • Clinical trial supply & packaging
    …highlights On-site CMC strategy and regulatory department pMDI pressure and cold filling Packaging and on-site QC laboratory Microbiology laboratories with extensive capabilities Pilot-sca…
  • Analytical testing
    …nsive capabilities Pilot-scale filling with any propellant (134a, 227ea, 152a and 1234ze) Analytical method development and validation BAI packaging At the heart of innovation Explore this facility…
  • Microbiology
    …regulatory department pMDI pressure and cold filling Packaging and on-site QC laboratory Microbiology laboratories with extensive capabilities Pilot-scale filling with any propellant (134a,…

Taken from the company's web page for this site. Source: https://www.kindevadd.com/facilities/loughborough-uk/, 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. 14 Mar 2025
    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 3002807586, inspection ID 1298022)

  2. 27 May 2021
    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 3002807586, inspection ID 1202201)

  3. 03 May 2018
    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 3002807586, inspection ID 1097508)

  4. 30 Jun 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 3002807586, inspection ID 1061585)

  5. 12 Aug 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 3002807586, inspection ID 982337)

  6. 05 Mar 2015
    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 3002807586, inspection ID 922069)

  7. 15 Apr 2013
    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 3002807586, inspection ID 827149)

  8. 17 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 3002807586, inspection ID 581481)

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.