FDA Investigator

Emmanuel Adu-Gyamfi

Latest inspection on record: Andover, United States, March 2023 · records back to 2022

Biologics

FDA inspection record · Last updated July 12, 2026

Overview

  • 5 inspections across 5 sites are on record.
  • 1 Form 483 observation is attributed to this investigator.
  • Most recent recorded activity is 2023-03-24.

At a glance

Inspections

5

Sites

5

Observations

1

Career since

Aug 2022

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Sarepta Therapeutics Inc24 Mar 2023BiologicsView 483 →
Catalent Maryland Inc10 Mar 2023BiologicsOn file
Catalent Maryland, Inc.24 Feb 2023Biologics
Biomarin Pharmaceutical Inc.9 Dec 2022BiologicsOn file
Uniqure Inc19 Aug 2022BiologicsOn file

Sites inspected

Sarepta Therapeutics IncAndover, United States1 insp.
Catalent Maryland IncHarmans, United States1 insp.
Catalent Maryland, Inc.Baltimore, United States1 insp.
Biomarin Pharmaceutical Inc.Novato, United States1 insp.
Uniqure IncLexington, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Sukyoung Sohn2 shared
Kevin J Matthews1 shared
Lilia L Bi1 shared
Ou Ma1 shared
Kula N Jha1 shared
Alifiya H Ghadiali1 shared

Full investigator report

Get the verbatim findings behind Emmanuel Adu-Gyamfi's 1 observation

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