FDA Investigator

Martin M Kimani

Latest inspection on record: Conyers, United States, March 2026 · records back to 2018

Human DrugsFoods & Cosmetics

FDA inspection record · Last updated July 12, 2026

Overview

  • 11 inspections across 11 sites are on record.
  • 29 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-03-26.

At a glance

Inspections

11

Sites

11

Observations

29

Career since

Mar 2018

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Newton Laboratories, Inc.26 Mar 2026Human DrugsOn file
Neogen Corporation6 Mar 2026Human DrugsOn file
American Regent, Inc.29 Jan 2026Human DrugsOn file
Smithfield Bioscience Inc23 Dec 2025Human DrugsOn file
Gojo Industries7 Nov 2025Human DrugsOn file

Sites inspected

Newton Laboratories, Inc.Conyers, United States1 insp.
Neogen CorporationLexington, United States1 insp.
American Regent, Inc.New Albany, United States1 insp.
Smithfield Bioscience IncCincinnati, United States1 insp.
Gojo IndustriesWooster, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Nelson N Ayangho1 shared
JoshRenzo N Ramilo1 shared
Robert J Ham1 shared
Craig P Seaborn1 shared

Full investigator report

Get the verbatim findings behind Martin M Kimani's 29 observations

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

Related investigators