FDA Investigator: Camille D. Brown

- Camille D. Brown first started conducting FDA inspections in 2013, with the last inspection in 2020. Over that time, Camille D. Brown has conducted 100 inspections at 97 companies across 97 sites.

Get Camille Brown's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.


Documents

Upon purchase, you will receive an email with a link to immediately download the documents.

FDA 483 Juan Jose Linares, MD, Granada | 2019

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Camille D. Brown
Human Drug Form 483

FDA 483 Viktor Vass, MD, Budapest Iii | 2019

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Camille D. Brown
Human Drug Form 483

FDA 483 ESPERION THERAPEUTICS INC, Ann Arbor | 2019

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Camille D. Brown
Human Drug Form 483

FDA 483 University of Texas at Arlington IRB, Arlington | 2019

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Camille D. Brown
Human Drug Form 483

FDA 483 Starpharma Pty Ltd, Abbotsford | 2018

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Camille D. Brown
Human Drug Form 483

FDA 483 Vanessa Chiapetta, MD, Austin | 2018

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Camille D. Brown
Foods & Cosmetic Form 483

FDA 483 Canadas, Rafael M.D., Dallas | 2018

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Camille D. Brown
Human Drug Form 483

FDA 483 Michael J. Downing, M.D., Dallas | 2018

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Camille D. Brown
Human Drug Form 483

FDA 483 Richard Dumas, Laval | 2018

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Camille D. Brown
Human Drug Form 483

FDA 483 Jerrold Grodin, MD, Dallas | 2018

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Camille D. Brown
Medical Devices & Rad Health Form 483

FDA 483 The Medical Center of Plano IRB, Plano | 2018

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Camille D. Brown
Medical Devices & Rad Health Form 483

FDA 483 Richard Buch, MD, Plano | 2017

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Camille D. Brown
Medical Devices & Rad Health Form 483

FDA 483 Kamran Khan, MD, Baytown | 2017

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Camille D. Brown
Human Drug Form 483