FDA Investigator

Madushini N Dharmasena

Latest inspection on record: Singapore, Singapore, May 2026 · records back to 2019

Human DrugsBiologics

FDA inspection record · Last updated July 12, 2026

Overview

  • 26 inspections across 25 sites are on record.
  • 0 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-05-05.

At a glance

Inspections

26

Sites

25

Observations

0

Career since

Mar 2019

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Thermo Fisher Biopharma Services PTE. LTD5 May 2026Human DrugsOn file
Q-Med AB27 Mar 2026Human DrugsOn file
Allergan Sales, LLC7 Nov 2025Human DrugsOn file
DR. REDDY'S LABORATORIES LTD12 Sep 2025Human DrugsOn file
GlaxoSmithKline Manufacturing S.p.A.15 May 2025Human DrugsOn file

Sites inspected

Thermo Fisher Biopharma Services PTE. LTDSingapore, Singapore1 insp.
Q-Med ABUppsala, Sweden1 insp.
Allergan Sales, LLCIrvine, United States1 insp.
DR. REDDY'S LABORATORIES LTDBachupally, India1 insp.
GlaxoSmithKline Manufacturing S.p.A.Torrile, Italy1 insp.

Co-investigators

Investigators who share inspections with this person.

Olumide A Martins2 shared
Ying Zhang2 shared
Maria G Gutierrez-Hoffman2 shared
Qibing Zhou1 shared
Jun Liu1 shared
Md Kamal Hossain1 shared
Baikuntha Aryal1 shared
Priscilla A Amador Do Amaral1 shared

Full investigator report

Get the verbatim findings behind Madushini N Dharmasena's inspection record

Source 483 PDFs, verbatim observations, and how each site responded, so your team knows what they cite before they arrive.

  • New inspections and Form 483s, mapped to the CFR citation
  • Warning letter outcomes, and the citation patterns they repeat
  • Their co-investigators, so no surprises about who shows up on site

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