Kathleen R. Jones
FDA Investigator
- Kathleen R. Jones first started conducting FDA inspections in 2017, with the last inspection in 2023. Over that time, Kathleen R. Jones has conducted 14 inspections at 13 companies across 14 sites.
Get Kathleen Jones'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 Recipharm AB, Oeiras | 2023
Out of stock
FDA 483 Novo Nordisk US Bio Production Inc., West Lebanon | 2020
Out of stock
FDA 483 Patheon Biologics B.V., Groningen | 2018
Out of stock
FDA 483 Boehringer Ingelheim Pharma Gmbh & Co Kg, Biberach an der Ris | 2017
Out of stock
Co-Investigators (22)
- Kula N. Jha, FDA Investigator
- Jessica Chery, FDA Investigator
- Unnee Ranjan, FDA Investigator
- Miriam M. Ngundi, FDA Investigator
- Lori P. Peters, FDA Investigator
- Anissa M. Cheung, FDA Investigator
- Ekaterina Allen, FDA Investigator
- Debra M. Emerson, FDA Investigator
- Arulvathani P. Arudchandran, FDA Investigator
- Wayne E. Seifert, FDA Investigator
- Maria J. Lopez- Barragan, FDA Investigator
- Lopez- Barragan, Maria J, FDA Investigator
- Brian D. Nicholson, FDA Investigator
- Diane L. Raccasi, FDA Investigator
- Scott R. Nichols, FDA Investigator
- Veronica Fuentes, FDA Investigator
- Richard Ledwidge, FDA Investigator
- Anh Lac, FDA Investigator
- Monica M. Commerford, FDA Investigator
- Yanming An, FDA Investigator
- Christopher D. Downey, FDA Investigator
- Bo Chi, FDA Investigator