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Bora Pharmaceuticals — Tao Yuan Shi

Tao Yuan Shi, Taiwan · CDMO

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

Site facts

Company
Bora Pharmaceuticals
Name(s) in FDA data
Bora Pharmaceutical Laboratories Inc. Zhongli Plant
FEI number(s)
3005674517 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Tao Yuan Shi, Taiwan
Records matched
4 FDA inspections
Most recent FDA inspection in dataset
07 Feb 2020 — VAI

Capabilities (from the company's website)

  • Oral solid dose
    …, Taiwan facility is designed for flexible, high-quality contract liquids, semi-solid and oral solid cGMP drug manufacturing. The facility offers best-in-class capabilities and access to the…
  • Oral liquids & semi-solids
    …e meter Zhongli, Taiwan facility is designed for flexible, high-quality contract liquids, semi-solid and oral solid cGMP drug manufacturing. The facility offers best-in-class capabilities an…

Taken from the company's web page for this site. Source: https://boracdmo.com/locations/zhongli/, 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. 07 Feb 2020
    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 3005674517, inspection ID 1119432)

  2. 13 Jul 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 3005674517, inspection ID 1061565)

  3. 15 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 3005674517, inspection ID 881386)

  4. 14 Sep 2012
    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 3005674517, inspection ID 801702)

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.