FDA Investigator

Jee Y Chung

Latest inspection on record: Clearwater, United States, January 2026 · records back to 2019

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 3 inspections across 3 sites are on record.
  • 4 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-01-09.

At a glance

Inspections

3

Sites

3

Observations

4

Career since

Jan 2019

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
QOL Medical LLC9 Jan 2026Human DrugsOn file
FujiFilm Diosynth Biotechnologies U.S.A., Inc.10 Feb 2023Human DrugsOn file
Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC17 Jan 2019Human DrugsView 483 →

Sites inspected

QOL Medical LLCClearwater, United States1 insp.
FujiFilm Diosynth Biotechnologies U.S.A., Inc.Research Triangle Park, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Hirdesh Kumar1 shared
Yi Wang1 shared
Zhong Li1 shared

Full investigator report

Get the verbatim findings behind Jee Y Chung's 4 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