FDA Investigator: Michelle M. Noe

- Michelle M. Noe first started conducting FDA inspections in 2002, with the last inspection in 2015. Over that time, Michelle M. Noe has conducted 225 inspections at 208 companies across 200 sites.

Get Michelle Noe'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 Andrea L. D. Orsey, M.D., Hartford | 2015

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Michelle M. Noe
Human Drug Form 483

FDA 483 Kent County Memorial Hospital Institutional Review Board, Warwick | 2015

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Michelle M. Noe
Human Drug Form 483

FDA 483 Steven P. Treon, M.D., PhD, Boston | 2014

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Michelle M. Noe
Human Drug Form 483

FDA 483 Christopher H. Comey, MD, Springfield | 2014

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Michelle M. Noe
Medical Devices & Rad Health Form 483

FDA 483 Suvranu Ganguli, MD, Boston | 2014

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Michelle M. Noe
Medical Devices & Rad Health Form 483

FDA 483 Ruth E. Tedaldi, MD, Wellesley Hills | 2014

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Michelle M. Noe
Medical Devices & Rad Health Form 483

FDA 483 Emerson Hospital Human Rights Committee, Concord | 2014

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Michelle M. Noe
Human Drug Form 483

FDA 483 Newton-Wellesley Hospital Human Research Committee, Wellesley Hills | 2014

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Michelle M. Noe
Medical Devices & Rad Health Form 483

FDA 483 Robert J. Weiss, M.D., Auburn | 2014

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Michelle M. Noe
Biologic Form 483

FDA 483 University of Rhode Island Institutional Review Board, Kingston | 2014

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Michelle M. Noe
Human Drug Form 483

FDA 483 Vimta Labs Limited, Hyderabad | 2014

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Michelle M. Noe
Human Drug Form 483

FDA 483 Avedro, Inc., Waltham | 2014

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Michelle M. Noe
Human Drug Form 483

FDA 483 Moussa C. Mansour, MD, Boston | 2013

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Michelle M. Noe
Medical Devices & Rad Health Form 483