FDA Investigator: Kelly N. Kerr
- Kelly N. Kerr first started conducting FDA inspections in 2016, with the last inspection in 2021. Over that time, Kelly N. Kerr has conducted 46 inspections at 44 companies across 43 sites.
Get Kelly Kerr'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 Sigrid Blome-Eberwein, Allentown | September 2020
Available Now - $199
Kelly N. Kerr
Human Drug Form 483
FDA 483 Paul R. Sieber, M.D, Lancaster | October 2019
Available Now - $199
Kelly N. Kerr
Human Drug Form 483
FDA 483 Ram K. Shrivastava, M.D, New York | July 2019
Available Now - $199
Kelly N. Kerr
Human Drug Form 483
FDA 483 Lawrence Levinson, M.D, Altoona | September 2018
Available Now - $199
Kelly N. Kerr
Human Drug Form 483
FDA 483 DERMDOX CENTERS FOR DERMATOLOGY, Sugarloaf | 2021
Out-of-stock
Kelly N. Kerr
Human Drug Form 483
FDA 483 Merck Sharp & Dohme Corp., West Point | 2019
Out-of-stock
Kelly N. Kerr
Human Drug Form 483
FDA 483 Abington Memorial Hospital,IRC, Abington | 2019
Out-of-stock
Kelly N. Kerr
Biologic Form 483
FDA 483 Erchonia Corporation, LLC, Melbourne | 2018
Out-of-stock
Kelly N. Kerr
Medical Devices & Rad Health Form 483
Co-Investigators (14)
- Melanie N. Daniels, FDA Investigator
- Gabrielle J. Swain, FDA Investigator
- Nina Yang, FDA Investigator
- Anastasia I. Offordile, FDA Investigator
- Stephanie C. Mangigian, FDA Investigator
- Mark J. Seaton, FDA Investigator
- Margaret E. Digennaro, FDA Investigator
- Brian S. Keefer, FDA Investigator
- Brandon J. Brookens, FDA Investigator
- Brandi L. Garbutt, FDA Investigator
- William C. Brenneman, FDA Investigator
- Maureen A. Wentzel, FDA Investigator
- Michael J. Mero, FDA Investigator
- Cara M. Minelli, FDA Investigator