FDA Investigator: Corey K. Reno

- Corey K. Reno first started conducting FDA inspections in 2010, with the last inspection in 2018. Over that time, Corey K. Reno has conducted 111 inspections at 98 companies across 98 sites.

Get Corey Reno'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 Hutchens Thomas MD, Bismarck | 2018

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Corey K. Reno
Medical Devices & Rad Health Form 483

FDA 483 Covance Laboratories, Inc., Madison | 2018

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Corey K. Reno
Human Drug Form 483

FDA 483 Avera Central Services IRB #3, Sioux Falls | 2018

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Corey K. Reno
Human Drug Form 483

FDA 483 Charles River Mattawan, Mattawan | 2018

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Corey K. Reno
Human Drug Form 483

FDA 483 Adrian Miranda, M.D., Milwaukee | 2018

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Corey K. Reno
Medical Devices & Rad Health Form 483

FDA 483 Dean Institutional Review Board, Madison | 2018

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Corey K. Reno
Human Drug Form 483

FDA 483 St Mary's Hospital IRB, Madison | 2017

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Corey K. Reno
Human Drug Form 483

FDA 483 Clinical Research Consortium, Tempe | 2017

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Corey K. Reno
Human Drug Form 483

FDA 483 Mercy Health System IRB, Janesville | 2017

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Corey K. Reno
Human Drug Form 483

FDA 483 Mayo Foundation IRB's, Rochester | 2017

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Corey K. Reno
Human Drug Form 483