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Kindeva Drug Delivery — Northridge

Northridge, California, United States · 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 L.P.
FEI number(s)
2010441 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Northridge, California, United States 91324
Records matched
12 FDA inspections · 6 inspections with posted 483 citations
Most recent FDA inspection in dataset
13 Nov 2025 — VAI

Capabilities (from the company's website)

  • Inhalation & nasal
    …tates Email - info@kindevadd.com Northridge highlights Full-service capabilities for pMDI/MDI and transdermal products pMDI/MDI pressure filling, cold filling and packaging 100M+ unit…
  • Clinical trial supply & packaging
    …ilities for pMDI/MDI and transdermal products pMDI/MDI pressure filling, cold filling and packaging 100M+ units per year Transdermal coating, converting and packaging On-site QC lab and cGM…

Taken from the company's web page for this site. Source: https://www.kindevadd.com/facilities/northridge-ca/, 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. 13 Nov 2025
    Form 483 observations 2 posted Form 483 citation(s)

    Citation summaries (2)
    • 21 CFR 211.110(a): Control procedures to monitor and validate performance
    • 21 CFR 211.192: No written record of investigation

    Source: FDA Data Dashboard – Citations (FEI 2010441, inspection ID 1286864)

  2. 13 Nov 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 2010441, inspection ID 1286864)

  3. 28 Jul 2021
    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 2010441, inspection ID 1151074)

  4. 25 Jan 2019
    Form 483 observations 2 posted Form 483 citation(s)

    Citation summaries (2)
    • 21 CFR 211.165(f): Failing drug products not rejected
    • 21 CFR 211.22(d): Procedures not in writing, fully followed

    Source: FDA Data Dashboard – Citations (FEI 2010441, inspection ID 1077108)

  5. 25 Jan 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 2010441, inspection ID 1082205)

  6. 25 Jan 2019
    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 2010441, inspection ID 1077108)

  7. 06 Mar 2017
    Form 483 observations 1 posted Form 483 citation(s)

    Citation summaries (1)
    • 21 CFR 211.160(b): Scientifically sound laboratory controls

    Source: FDA Data Dashboard – Citations (FEI 2010441, inspection ID 1008836)

  8. 06 Mar 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 2010441, inspection ID 1008836)

  9. 01 Sep 2015
    Form 483 observations 3 posted Form 483 citation(s)

    Citation summaries (3)
    • 21 CFR 211.110(a): Control procedures to monitor and validate performance
    • 21 CFR 211.160(b): Scientifically sound laboratory controls
    • 21 CFR 211.180(e)(1): Review of representative number of batches

    Source: FDA Data Dashboard – Citations (FEI 2010441, inspection ID 940328)

  10. 01 Sep 2015
    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 2010441, inspection ID 940328)

  11. 17 Sep 2014
    Form 483 observations 1 posted Form 483 citation(s)

    Citation summaries (1)
    • 21 CFR 211.68(b): Computer control of master formula records

    Source: FDA Data Dashboard – Citations (FEI 2010441, inspection ID 896244)

  12. 17 Sep 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 2010441, inspection ID 896244)

  13. 23 Aug 2013
    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 2010441, inspection ID 845595)

  14. 04 Jan 2012
    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 2010441, inspection ID 761084)

  15. 05 Nov 2010
    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 2010441, inspection ID 702983)

  16. 12 Feb 2010
    Form 483 observations 2 posted Form 483 citation(s)

    Citation summaries (2)
    • 21 CFR 211.100(b): SOPs not followed / documented
    • 21 CFR 211.67(b): Written procedures fail to include

    Source: FDA Data Dashboard – Citations (FEI 2010441, inspection ID 645889)

  17. 12 Feb 2010
    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 2010441, inspection ID 645889)

  18. 02 Feb 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 2010441, inspection ID 565497)

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.