FDA Investigator: Sheri S. Oliver
- Sheri S. Oliver first started conducting FDA inspections in 2008, with the last inspection in 2018. Over that time, Sheri S. Oliver has conducted 54 inspections at 51 companies across 54 sites.
Get Sheri Oliver'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 Conrado Estol, M.D., Buenos Aires | 2018
Out-of-stock
Sheri S. Oliver
Human Drug Form 483
FDA 483 Delia Chaverri, M.D., Madrid | 2017
Out-of-stock
Sheri S. Oliver
Human Drug Form 483
FDA 483 Angel Leon, MD, Atlanta | 2012
Out-of-stock
Sheri S. Oliver
Medical Devices & Rad Health Form 483
FDA 483 Brian Bortnick, Atlanta | 2012
Out-of-stock
Sheri S. Oliver
Human Drug Form 483
Co-Investigators (20)
- Kassa Ayalew, FDA Investigator
- Phillip D. Kronstein, FDA Investigator
- Barbara D. Wright, FDA Investigator
- Lareese K. Thomas, FDA Investigator
- Katrina B. Mosley, FDA Investigator
- Seneca D. Toms, FDA Investigator
- Viviana Matta, FDA Investigator
- Myla D. Chapman, FDA Investigator
- Michelle D. Haamid, FDA Investigator
- Barbara M. Frazier, FDA Investigator
- Kimberly C. Delk-Brooks, FDA Investigator
- Gabriel R. McLemore, FDA Investigator
- Cordelia J. Brammer, FDA Investigator
- Ingrid A. Zambrana, FDA Investigator
- Brandy Davis Brown, FDA Investigator
- Davis Brown, Brandy, FDA Investigator
- Leslie W. Gilbert, FDA Investigator
- Hai Lien Phung, FDA Investigator
- Phung, Hai Lien T, FDA Investigator
- Gamal A. Norton, FDA Investigator