Christine E. Kelley
FDA Investigator
- Christine E. Kelley first started conducting FDA inspections in 2007, with the last inspection in 2024. Over that time, Christine E. Kelley has conducted 66 inspections at 58 companies across 61 sites.
Get Christine Kelley'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 Excalibur Lipid Technology, Inc., Memphis | 2024
Out of stock
FDA 483 Fidia Farmaceutici S.p.A., Abano Terme | 2016
Out of stock
FDA 483 Pristine Bay LLC, Blue Ash | 2015
Out of stock
FDA 483 Standard Textile Co Inc, Cincinnati | 2013
Out of stock
FDA 483 KBD, Inc., Crescent Springs | 2012
Out of stock
FDA 483 SRI/ Surgical Express Inc, Mason | 2012
Out of stock
FDA 483 Casco Manufacturing Solutions Inc, Cincinnati | 2012
Out of stock
FDA 483 Basic Organics Inc, Columbus | 2012
Out of stock
Co-Investigators (20)
- Thunder N. Dunkijacobs, FDA Investigator
- Tracey L. Harris, FDA Investigator
- Maribeth G. Niesen, FDA Investigator
- Richard W. Berning, FDA Investigator
- Jennifer L. Jager, FDA Investigator
- Lindsey M. Schwierjohann, FDA Investigator
- Roy C. Stephens, FDA Investigator
- Allison M. Scheck, FDA Investigator
- Elizabeth P. Kinsella, FDA Investigator
- Elizabeth L. Edwards, FDA Investigator
- Brigitte K. Hofmann, FDA Investigator
- Anna M. Brannen, FDA Investigator
- Javonica F. Penn, FDA Investigator
- Laureen M. Geniusz, FDA Investigator
- Christopher T. Middendorf, FDA Investigator
- Michael E. Campbell, FDA Investigator
- William K. Ducloux, FDA Investigator
- David P. Moorhead, FDA Investigator
- John D. Jaworski, FDA Investigator
- Bryan J. Love, FDA Investigator