FDA Investigator: Kathleen R. Jones
- 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 Wyeth BioPharma Division of Wyeth Pharmaceuti | 2021
Available Now - $199
Kathleen R. Jones
Biologic Form 483
FDA EIR Adello Biologics, Chicago | November 2017
Available Now - $995
Kathleen R. Jones
Human Drug Form 483
FDA 483 BioMarin International, Ringaskiddy | May 2017
Available Now - $199
Kathleen R. Jones
Human Drug Form 483
FDA 483 Novo Nordisk US Bio Production Inc., West Lebanon | 2020
Out-of-stock
Kathleen R. Jones
Biologic Form 483
FDA 483 Patheon Biologics B.V., Groningen | 2018
Out-of-stock
Kathleen R. Jones
Human Drug Form 483
FDA 483 Boehringer Ingelheim Pharma Gmbh & Co Kg, Biberach an der Ris | 2017
Out-of-stock
Kathleen R. Jones
Human Drug Form 483
Co-Investigators (22)
- Kula N. Jha, FDA Investigator
- Jessica Chery,
- 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