FDA Investigator

Jean M Mulinde

Latest inspection on record: Hatfield, United Kingdom, February 2019 · records back to 2015

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 7 inspections across 6 sites are on record.
  • 11 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2019-02-01.

At a glance

Inspections

7

Sites

6

Observations

11

Career since

Dec 2015

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Eisai Manufacturing Ltd1 Feb 2019Human DrugsView 483 →
AstraZeneca Pharmaceuticals LP11 Oct 2018Human Drugs
Eisai, Inc.16 Feb 2018Human DrugsView 483 →
Rho, Inc.30 Jun 2017Human DrugsView 483 →
Ironshore Pharmaceuticals & Development, Inc.7 Mar 2017Human Drugs

Sites inspected

Eisai Manufacturing LtdHatfield, United Kingdom1 insp.
AstraZeneca Pharmaceuticals LPGaithersburg, United States1 insp.
Eisai, Inc.Nutley, United States1 insp.
Rho, Inc.Chapel Hill, United States1 insp.
Ironshore Pharmaceuticals & Development, Inc.Grand Cayman, Cayman Islands1 insp.

Co-investigators

Investigators who share inspections with this person.

Lauren C Iacono-Connors2 shared
Nina Yang2 shared
Bei Yu1 shared
David L Chon1 shared

Full investigator report

Get the verbatim findings behind Jean M Mulinde's 11 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