FDA Investigator

Olumide A Martins

Latest inspection on record: Uppsala, Sweden, March 2026 · records back to 2024

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 6 inspections across 6 sites are on record.
  • 0 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-03-27.

At a glance

Inspections

6

Sites

6

Observations

0

Career since

Mar 2024

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Q-Med AB27 Mar 2026Human DrugsOn file
GlaxoSmithKline Manufacturing S.p.A.15 May 2025Human DrugsOn file
GlaxoSmithKline LLC7 Mar 2025Human DrugsOn file
KBI Biopharma, Inc.18 Jun 2024Human DrugsOn file
KBI Biopharma, Inc.17 Jun 2024Human Drugs

Sites inspected

Q-Med ABUppsala, Sweden1 insp.
GlaxoSmithKline LLCConshohocken, United States1 insp.
KBI Biopharma, Inc.Durham, United States1 insp.
KBI Biopharma, Inc.Durham, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Qibing Zhou1 shared
Jun Liu1 shared
Shadia Zaman1 shared
Sarah A Johnson1 shared

Full investigator report

Get the verbatim findings behind Olumide A Martins' 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