FDA Investigator Lei Zhang, PhD

Lei Zhang, PhD has conducted inspections on 5 sites in 3 countries as of 06 Mar 2023. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
5
Last Inspection Date:
06 Mar 2023
Investigator Role:
FDA Investigator
Redica ID:
100007949
Countries of Inspections:
United States of America, Iceland, Taiwan
FDA Investigators that have inspected at least one site in common with Lei Zhang, PhD:
Adam R Cooke, Amy C Jordan, Amy N Chen, Arsen Karapetyan, Bingchen Du, PhD, Bonita S Chester, Burnell M Henry, Calvin B Koerner, Cathleen A Carr Sharpe, CDR Thomas R Berry, PPh, Cynthia Jim, CSO, Daryl A Dewoskin, Devaughn Edwards, Dien N Nguyen, Donald C Obenhuber, PhD, Dr. Ralph M Bernstein, PhD, Dr. Zhihao Qiu (Peter), PhD, Edmund F Mrak, Jr, Gilbert T Salud, Hai Lient Phung, Hamet M Toure, PharmD MPH, Ibad U Khan, Jacek Cieslak, PhD, James R Evans, Jason F Chancey, Jeffrey P Raimondi, Jie He, Jose Acruz Gonzalez, José E Meléndez, Joseph F Owens, Joseph Kutze, PhD, Julie D Bringger, Karen A Briggs, Kirsten L Vadheim, PhD, Laura I Salazar, PhD, Leiyun Boone, PhD, Lois K Gross, Madushini Dharmasena, PhD, Maria Joselopez Barragan, PhD, Marion Michaelis, Mark R Mcclain, Megan A Haggerty, Michael Shanks, MS, Michelle Yclark Stuart, Mihaly S Ligmond, Nealie C Newberger, Prabhu P Raju, Priscilla M Pastrana, Rebecca Rodriguez, Reyes Candau Chacon, PhD, Richard Ledwidge (nmi), PhD, Robert D Tollefsen, Robert Jennings, Scott C Lute, Sean R Marcsisin, Seneca D Toms, Sidney B Priesmeyer, Stacey S Degarmo, Steven Fong, MS, PhD, Susan M Jackson, Tamara M Casselman, Thuy T Nguyen, LCDR, Viviana Matta, Wayne E Seifert, William Hallett, PhD, Yetao Jin, PhD, Zhao Wang, PhD, Ziyang Su, PhD

Lei Zhang, PhD's Documents

Publish Date Document Type Title
April, 2019 FDA 483 Immunex Rhode Island Corporation - Form 483, 2019-04-19
August, 2004 EIR Biogen Idec, Inc. - EIR, 2004-11-05
August, 2004 EIR Biogen MA Inc. - EIR, 2004-08-27
March, 2023 FDA 483 Alvotech Hf - Form 483, 2023-03-17

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