FDA Investigator: Kellie Leveille
- Kellie Leveille first started conducting FDA inspections in 2015, with the last inspection in 2017. Over that time, Kellie Leveille has conducted 30 inspections at 28 companies across 27 sites.
Get Kellie Leveille'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 Libera Medical, PLLC, New York | 2016
Out-of-stock
Kellie Leveille
Biologic Form 483
FDA 483 M.A.Z.E. Laboratories, Purchase | 2016
Out-of-stock
Kellie Leveille
Biologic Form 483
FDA 483 New Hope Fertility Center, New York | 2016
Out-of-stock
Kellie Leveille
Biologic Form 483
FDA 483 Offices for Fertility and Reproductive Medicine, P. C., New York | 2016
Out-of-stock
Kellie Leveille
Biologic Form 483
FDA 483 Repro Lab, New York | 2016
Out-of-stock
Kellie Leveille
Biologic Form 483
Co-Investigators (12)
- Irina Gaberman, FDA Investigator
- Amy W. Yan Mai, FDA Investigator
- Yan Mai, Amy W, FDA Investigator
- Mercedes G. Castillo, FDA Investigator
- Dave M. Deroche, FDA Investigator
- Tara K. Carmody, FDA Investigator
- Christian Parra, FDA Investigator
- Raymond M. Lam, FDA Investigator
- Duo D. Chen, FDA Investigator
- Nada F. Agabani, FDA Investigator
- Valerie A. Potopsingh, FDA Investigator
- Iram R. Hassan, FDA Investigator