FDA Investigator: Kara A. Scheibner
- Kara A. Scheibner first started conducting FDA inspections in 2017, with the last inspection in 2024. Over that time, Kara A. Scheibner has conducted 25 inspections at 25 companies across 25 sites.
Get Kara Scheibner'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 Armstrong Pharmaceuticals, Inc., Canton | 2024
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Kara A. Scheibner
Human Drugs Form 483
FDA 483 Sitec Labs Limited, Navi Mumbai | 2024
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Kara A. Scheibner
Human Drugs Form 483
FDA 483 Solvias AG, Kaiseraugst | 2023
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Kara A. Scheibner
Human Drugs Form 483
FDA 483 Raptim Research Pvt. Ltd., Navi Mumbai | 2023
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Kara A. Scheibner
Human Drugs Form 483
FDA 483 Synchron Research Services Pvt. Ltd., Ahmedabad | 2019
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Kara A. Scheibner
Human Drug Form 483
FDA 483 Charles River Laboratories Ashland, LLC, Skokie | 2019
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Kara A. Scheibner
Human Drug Form 483
FDA 483 Keystone Bioanalytical, Inc., North Wales | 2019
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Kara A. Scheibner
Human Drug Form 483
FDA 483 Raptim Research Ltd, Navi Mumbai | 2019
Out-of-stock
Kara A. Scheibner
Human Drug Form 483
FDA 483 Dana-Farber Harvard Cancer Center, Boston | 2018
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Kara A. Scheibner
Human Drug Form 483
FDA 483 inVentiv Health Clinical Lab, Inc., Princeton | 2017
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Kara A. Scheibner
Human Drug Form 483
Co-Investigators (14)
- Kent A. Conforti, FDA Investigator
- Sylvestre K. Dossou,
- Hasan A. Irier, FDA Investigator
- Makini Cobourne-Duval, FDA Investigator
- Michael P. Anthony, FDA Investigator
- Jeanne J. Thai, FDA Investigator
- Joseph L. Despins, FDA Investigator
- Li-Hong P. Yeh, FDA Investigator
- Li-Hong Yeh, FDA Investigator
- Amanda Lewin, FDA Investigator
- Denise L. Burosh, FDA Investigator
- Xiaohan Cai, FDA Investigator
- Gajendiran Mahadevan, FDA Investigator
- Thea C. Grome, FDA Investigator