FDA Investigator: Scott E. Norris
- Scott E. Norris first started conducting FDA inspections in 2017, with the last inspection in 2019. Over that time, Scott E. Norris has conducted 4 inspections at 4 companies across 4 sites.
Get Scott Norris'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 Wyeth Pharmaceutical Division of Wyeth Holdings LLC, Sanford | 2019
Out-of-stock
Scott E. Norris
Biologic Form 483
FDA 483 Merck Sharp & Dohme Corp., West Point | 2019
Out-of-stock
Scott E. Norris
Biologic Form 483
FDA 483 Pfizer Ireland Pharmaceuticals, Dublin 22 | 2018
Out-of-stock
Scott E. Norris
Biologic Form 483
FDA 483 Sanofi Pasteur SA, Marcy L Etoile | 2017
Out-of-stock
Scott E. Norris
Biologic Form 483
Co-Investigators (10)
- Jacqueline M. Diaz Albert, FDA Investigator
- Brentley S. Collins, FDA Investigator
- Diaz Albert, Jacqueline M, FDA Investigator
- Prabhu P. Raju, FDA Investigator
- Christopher J. Adams, FDA Investigator
- Anissa M. Cheung, FDA Investigator
- Eileen A. Liu, FDA Investigator
- Linda Thai, FDA Investigator
- Mihaly S. Ligmond, FDA Investigator
- Michele L. Forster, FDA Investigator