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BioVectra — Charlottetown

Charlottetown, Canada · CDMO

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

Site facts

Company
BioVectra
Name(s) in FDA data
Biovectra, Inc.
FEI number(s)
3004063541 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Charlottetown, Canada
Records matched
7 FDA inspections
Most recent FDA inspection in dataset
19 Apr 2024 — VAI

Capabilities (from the company's website)

  • Biologics drug substance
    …Charlottetown, Prince Edward Island Biologics manufacturing in…

Taken from the part of the company's network/locations page that describes this site. Source: https://www.biovectra.com/facilities/, 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. 19 Apr 2024
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Veterinary. Project area(s): Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 3004063541, inspection ID 1239225)

  2. 26 Aug 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 3004063541, inspection ID 1180023)

  3. 17 Feb 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 3004063541, inspection ID 1008484)

  4. 17 Apr 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 3004063541, inspection ID 927704)

  5. 08 Aug 2013
    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 3004063541, inspection ID 847468)

  6. 25 Aug 2010
    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 3004063541, inspection ID 684938)

  7. 25 Aug 2010
    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 3004063541, inspection ID 684844)

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.