FDA Investigator: Emily E. Smith
- Emily E. Smith first started conducting FDA inspections in 2000, with the last inspection in 2008. Over that time, Emily E. Smith has conducted 152 inspections at 85 companies across 92 sites.
Get Emily Smith'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 Interstate Blood Bank Inc, Memphis | 2008
Out-of-stock
Emily E. Smith
Biologic Form 483
FDA 483 CSL Plasma Inc., Memphis | 2007
Out-of-stock
Emily E. Smith
Biologic Form 483
FDA 483 Wright Medical Technology Inc, Arlington | 2006
Out-of-stock
Emily E. Smith
Medical Devices & Rad Health Form 483
FDA 483 University of Tennessee Health Science Center IRB, Memphis | 2006
Out-of-stock
Emily E. Smith
Human Drug Form 483
Co-Investigators (14)
- Jean A. Peeples, FDA Investigator
- Cntrctmntr Briggs, FDA Investigator
- Michael T. Nehring, FDA Investigator
- Thomas R. Stanley, FDA Investigator
- Lawrence A. Butler, FDA Investigator
- Holly I. Hall, FDA Investigator
- Steven D. Dittert, FDA Investigator
- Leon T. Morgan, FDA Investigator
- David R. Heiar, FDA Investigator
- William P. Chatham, FDA Investigator
- Kimberly L. McMillan, FDA Investigator
- Kenneth R. Merritt, FDA Investigator
- Joan A. Loreng, FDA Investigator
- Brian S. Lynch, FDA Investigator