FDA Investigator: Scott R. Nichols
- Scott R. Nichols first started conducting FDA inspections in 2016, with the last inspection in 2019. Over that time, Scott R. Nichols has conducted 11 inspections at 11 companies across 11 sites.
Get Scott Nichols'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 Catalent Indiana, Bloomington | May 2018
Available Now - $199
Scott R. Nichols
Human Drug Form 483
FDA 483 Chiesi Farmaceutici S.p.A., Parma | 2019
Out-of-stock
Scott R. Nichols
Human Drug Form 483
FDA 483 Lonza Biologics Plc, Slough | 2018
Out-of-stock
Scott R. Nichols
Human Drug Form 483
FDA 483 KBI Biopharma, Inc., Boulder | 2018
Out-of-stock
Scott R. Nichols
Human Drug Form 483
FDA 483 Kyowa Hakko Kirin Co., Ltd., Takasaki | 2017
Out-of-stock
Scott R. Nichols
Human Drug Form 483
FDA 483 Sandoz GmbH, Langkampfen | 2017
Out-of-stock
Scott R. Nichols
Human Drug Form 483
FDA 483 Biocon Limited, Work Site I, Hebbagodi Bangalore | 2017
Out-of-stock
Scott R. Nichols
Human Drug Form 483
FDA 483 Merck Serono SA (Vevey), Corsier-sur-Vevey | 2016
Out-of-stock
Scott R. Nichols
Human Drug Form 483
Co-Investigators (10)
- Saleem A. Akhtar, FDA Investigator
- Steven Fong, FDA Investigator
- Ralph M. Bernstein, FDA Investigator
- Jamie L. Dion, FDA Investigator
- Nicholas L. Paulin, FDA Investigator
- Thuy T. Nguyen, FDA Investigator
- Zhong Li, FDA Investigator
- Kathleen R. Jones, FDA Investigator
- Michael Shanks, FDA Investigator
- Reyes Candau-Chacon, FDA Investigator