FDA Investigator: Christine E. Kelley
- 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 Innovative Sterlization Technologies, Dayton | 2014
Available Now - $199
Christine E. Kelley
Medical Devices & Rad Health Form 483
FDA 483 Tango3, Simpsonville | July 2014
Available Now - $199
Christine E. Kelley
Medical Devices & Rad Health Form 483
FDA 483 Excalibur Lipid Technology, Inc., Memphis | 2024
Out-of-stock
Christine E. Kelley
Foods & Cosmetics Form 483
FDA 483 Fidia Farmaceutici S.p.A., Abano Terme | 2016
Out-of-stock
Christine E. Kelley
Medical Devices & Rad Health Form 483
FDA 483 Pristine Bay LLC, Blue Ash | 2015
Out-of-stock
Christine E. Kelley
Foods & Cosmetic Form 483
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