FDA Investigator: Jean M. Mulinde
- Jean M. Mulinde first started conducting FDA inspections in 2015, with the last inspection in 2019. Over that time, Jean M. Mulinde has conducted 7 inspections at 6 companies across 6 sites.
Get Jean Mulinde'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 Eisai Manufacturing Limited, Hatfield | 2019
Out-of-stock
Jean M. Mulinde
Human Drug Form 483
FDA 483 Eisai, Inc., Woodcliff Lake | 2018
Out-of-stock
Jean M. Mulinde
Human Drug Form 483
FDA 483 Rho, Inc., Chapel Hill | 2017
Out-of-stock
Jean M. Mulinde
Human Drug Form 483
FDA 483 Merck Sharp & Dohme, Rahway | 2016
Out-of-stock
Jean M. Mulinde
Human Drug Form 483
Co-Investigators (11)
- Craig A. Garmendia, FDA Investigator
- Melanie N. Daniels, FDA Investigator
- David L. Chon, FDA Investigator
- Robin R. Waller, FDA Investigator
- Bei Yu, FDA Investigator
- Nina Yang, FDA Investigator
- Peter R. Lenahan, FDA Investigator
- Lauren C. Iacono-Connors, FDA Investigator
- Michael Serrano, FDA Investigator
- Jenn W. Sellers, FDA Investigator
- Shirley S. Wen, FDA Investigator