FDA Investigator

Hamet M Toure

Latest inspection on record: East Greenbush, United States, January 2026 · records back to 2022

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 17 inspections across 17 sites are on record.
  • 0 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-01-16.

At a glance

Inspections

17

Sites

17

Observations

0

Career since

Aug 2022

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Regeneron Pharmaceuticals, Inc.16 Jan 2026Human DrugsOn file
Lupin Limited19 Sep 2025Human DrugsOn file
GlaxoSmithKline LLC7 Mar 2025Human DrugsOn file
Intas Pharmaceuticals Limited14 Feb 2025Human DrugsOn file
CELLTRION Inc14 Jan 2025Human Drugs

Sites inspected

Regeneron Pharmaceuticals, Inc.East Greenbush, United States1 insp.
Lupin LimitedPune, India1 insp.
GlaxoSmithKline LLCConshohocken, United States1 insp.
Intas Pharmaceuticals LimitedMoraiya, India1 insp.
CELLTRION IncYeonsu District, Korea (the Republic of)1 insp.

Co-investigators

Investigators who share inspections with this person.

Jiangsong Jiang1 shared
Prabuddha Sengupta1 shared
Shadia Zaman1 shared
Karthik M Krishnan1 shared
Olumide A Martins1 shared
Bingchen Du1 shared
Doan N Singh1 shared

Full investigator report

Get the verbatim findings behind Hamet M Toure'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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