FDA Investigator: Vickie J. Kanion
- Vickie J. Kanion first started conducting FDA inspections in 2009, with the last inspection in 2020. Over that time, Vickie J. Kanion has conducted 153 inspections at 130 companies across 137 sites.
Get Vickie Kanion'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 Anuj Bhargava MD, West Des Moines | December 2020
Available Now - $199
Vickie J. Kanion
Human Drug Form 483
FDA 483 Joel Schlessinger, M.D, Omaha | December 2019
Available Now - $199
Vickie J. Kanion
Human Drug Form 483
FDA 483 Thomas Sutton, MD, Highland | May 2018
Available Now - $199
Vickie J. Kanion
Medical Devices & Rad Health Form 483
FDA 483 John Meadors, Highland | May 2018
Available Now - $199
Vickie J. Kanion
Medical Devices & Rad Health Form 483
Co-Investigators (25)
- Joshua R. Hayes, FDA Investigator
- Michael F. Skelly, FDA Investigator
- Stephen T. Hansen, FDA Investigator
- Yiyue Zhang, FDA Investigator
- Ruben C. Ayala, FDA Investigator
- Eric T. Huebler, FDA Investigator
- Lisa D. Ellis, FDA Investigator
- Lisa L. Flores, FDA Investigator
- Don A. Leeseberg, FDA Investigator
- Kevin A. Beavers, FDA Investigator
- Thomas K. Dobbs, FDA Investigator
- Linda R. Kuchenthal, FDA Investigator
- Susanna E. Ford, FDA Investigator
- Jessica L. Peterson, FDA Investigator
- Julie N. Vosilus, FDA Investigator
- William F. Lagud, FDA Investigator
- Cody D. Rickman, FDA Investigator
- Carmen Y. Fisher, FDA Investigator
- Sarah E. Morris, FDA Investigator
- Farhana Khan, FDA Investigator
- Lisa L. Gilliam, FDA Investigator
- Richard L. Rutherford, FDA Investigator
- Melva J. Palmer, FDA Investigator
- Fenhong Song, FDA Investigator
- Erin C. Dugan, FDA Investigator