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PolyPeptide — Strasbourg

Strasbourg, France · CDMO

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

Site facts

Company
PolyPeptide
Name(s) in FDA data
Polypeptide Laboratories France
FEI number(s)
3007417577 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Strasbourg, France
Records matched
4 FDA inspections
Most recent FDA inspection in dataset
04 Jul 2024 — VAI

Capabilities (from the company's website)

  • Lyophilization
    …0L in capacity. The facility has 8 independent purification and isolation suites. Several lyophilizers are available with capacities up to 200 kg of ice. This site manufactures proprietary…
  • Peptides & oligonucleotides
    …PolyPeptide Strasbourg, France The Strasbourg, France site is a 65,000 square foot (~6,500 sq. meters…

Taken from the company's web page for this site. Source: https://www.polypeptide.com/contacts/manufacturing-sites/strasbourg-france/, 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. 04 Jul 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 3007417577, inspection ID 1280973)

  2. 12 Sep 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 3007417577, inspection ID 1107059)

  3. 23 May 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 3007417577, inspection ID 884800)

  4. 16 Sep 2009
    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 3007417577, inspection ID 620930)

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.