FDA Investigator Scott J Lewis
Scott J Lewis has conducted inspections on 6 sites in 2 countries as of 11 Dec 2023. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
6
Last Inspection Date:
11 Dec 2023
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Japan
FDA Investigators that have inspected at least one site in common with Scott J Lewis:
Billy M Battles,
Binh T Nguyen,
Cullen T Wilson,
Daniel J Gorski,
Erika V Butler,
Gabriel M Guevarra,
Gale L Glinecki,
Himabindu Mandyam,
Karen E D'orazio,
Liatte Kreuger, PharmD,
Margaret E Walsh,
Melissa D Ray,
Michael R Klapal,
Nicholas A Violand,
Richard L Garcia,
Theresa L Stewart,
Tonia F Bernard,
Zachary A Bogorad,
Zachary L Miller
Scott J Lewis's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2018 | FDA 483 | The University of Utah DBA Cyclotron Radiochemistry Lab Huntsman Cancer Institute - Form 483, 2018-08-30 |
March, 2011 | FDA 483 | Spring Hope Poultry - Form 483, 2011-03-23 |
Experience Redica Systems’ NEW investigator profiles and dashboards
Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:
- Total inspections conducted
- 483 rate
- OAI rate
- Warning Letter rate
- Inspections by Industry, Scope, and Inspection Reason
- And much more
Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.
![FDA Investigator Profile Icon](/images/InspectorProfile.png)
Talk to sales to access our investigator profiles
Loading...
Investigator Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:
Inspection Intelligence
- Pre-Approval Inspection (PAI) trends
- The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
- Latest 483s: see what the trends are across all FDA Investigators
- CFR Heatmap: Citations aggregated by Subpart by Year
Vendor Intelligence
- Full inspection histories for your vendors down to the specific site level
- All of the functionality mentioned above but isolated to just your vendors
Regulatory Intelligence
- Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
- All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more