FDA Investigator: Dana M. Klimavicz
- Dana M. Klimavicz first started conducting FDA inspections in 2000, with the last inspection in 2024. Over that time, Dana M. Klimavicz has conducted 342 inspections at 239 companies across 234 sites.
Get Dana Klimavicz'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 Jonathan K. Wise, M.D, Metairie | December 2017
Available Now - $199
Dana M. Klimavicz
Human Drug Form 483
FDA 483 Baton Rouge General Medical Center IRB, Baton Rouge | 2023
Out-of-stock
Dana M. Klimavicz
Biologics Form 483
FDA 483 Wayne J.G. Hellstrom, M.D., New Orleans | 2018
Out-of-stock
Dana M. Klimavicz
Human Drug Form 483
Co-Investigators (20)
- Christopher M. Jeffers, FDA Investigator
- Matthew R. Coleman, FDA Investigator
- Barbara D. Wright, FDA Investigator
- Diane Hall, FDA Investigator
- Abby L. Mozeke-Baker, FDA Investigator
- Mary I. Surratt, FDA Investigator
- Patrick C. Dooley, FDA Investigator
- Wayne S. Fortenberry, FDA Investigator
- Bonnie E. Pierson, FDA Investigator
- Kip J. Hanks, FDA Investigator
- Teresa Bills, FDA Investigator
- Samantha J. Bradley, FDA Investigator
- Daphne A. Videau, FDA Investigator
- Stephanie A. Cochran, FDA Investigator
- Juanelma H. Palmer, FDA Investigator
- Elizabeth D. Connell, FDA Investigator
- Natalie A. Guidry, FDA Investigator
- Charles N. Dupont, FDA Investigator
- Sidney M. Smith, FDA Investigator
- Francis A. Guidry, FDA Investigator