Directory › Delpharm

Delpharm — Huningue

Huningue, France · CDMO

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

Site facts

Company
Delpharm
Name(s) in FDA data
Delpharm Huningue S.A.S.
FEI number(s)
3003157245 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Huningue, France
Records matched
6 FDA inspections · 1 inspection with posted 483 citations
Most recent FDA inspection in dataset
30 Nov 2023 — VAI

Capabilities (from the company's website)

  • Oral liquids & semi-solids
    …Huningue plant Solid dosage forms L’aigle Plant Leiden development center Semi-solid and liquid dosage forms…

Taken from the part of the company's network/locations page that describes this site. Source: https://www.delpharm.com/en/our-sites/sites-france-europe/, 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. 30 Nov 2023
    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 3003157245, inspection ID 1262708)

  2. 08 Aug 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 3003157245, inspection ID 1125617)

  3. 22 Jun 2018
    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 3003157245, inspection ID 1060634)

  4. 23 Sep 2016
    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 3003157245, inspection ID 988001)

  5. 19 Dec 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 3003157245, inspection ID 913598)

  6. 15 Dec 2011
    Form 483 observations 3 posted Form 483 citation(s)

    Citation summaries (3)
    • 21 CFR 211.113(a): Procedures for non-sterile drug products
    • 21 CFR 211.68(a): Calibration/Inspection/Checking not done
    • 21 CFR 211.84(d)(2): Establish reliability of supplier's C of A

    Source: FDA Data Dashboard – Citations (FEI 3003157245, inspection ID 765433)

  7. 15 Dec 2011
    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 3003157245, inspection ID 765433)

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.