FDA Investigator: Jee Y. Chung
- Jee Y. Chung first started conducting FDA inspections in 2019, with the last inspection in 2023. Over that time, Jee Y. Chung has conducted 2 inspections at 2 companies across 2 sites.
Get Jee Chung's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.
Documents
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FDA 483 FujiFilm Diosynth Biotechnologies U.S.A., Inc., Research Triangle Park | 2023
Out-of-stock
Jee Y. Chung
Human Drugs Form 483
FDA 483 Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC, Andover | 2019
Out-of-stock
Jee Y. Chung
Human Drug Form 483