FDA Investigator Josiah D Davis
Josiah D Davis has conducted inspections on 20 sites in 1 countries as of 25 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
20
Last Inspection Date:
25 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Josiah D Davis:
Alissa C Rice,
Andrew M Kupper,
Andrew Saunders,
Anna E Fain,
Chantel Evans Dixon,
Cheryl G Scott,
Christian L Witkovskie,
Claire M Minden,
Clifton C Francis,
Combs,
Craig P Seaborn,
Dawn P Hall,
Debra A Sherman,
Decima L Washington,
Dyanthony T Jenkins,
George J Flynn,
Grant D Jones,
Javonica F Penn,
Jessica M Wooten,
John E Russell, Jr,
Karen M Cooper,
Kathryn Suttling,
Kerry Ann Latham,
Kimberly A Joseph,
Kimberly L Mcmillan,
Kip J Hanks,
Krista T Ferry,
Lacey J Chessor,
Lakisha N Morton,
Linda A Gregory Duty,
Lindsay H Bertling,
Luckner Jean Marie,
Maressa L Mills,
Marissa R Stough,
Markeesa M Scales,
Marshall H Kinsey,
Marvin D Jones,
Mary B Sheets,
Matthew G Ellison,
Meocha V Whaley,
Peggy A Stogner,
Samuel L Collins,
Sandricka M Mosley,
Sandy L Atkins,
Sarah M Parkinson,
Shalonda L Gatewood,
Shannon Atlas,
Shelton L Stribling,
Shondra N Gipson,
Sidney M Smith,
Stephen G Mclane,
Steven D Dittert,
Talmane J Fisher,
Thomas B Smith,
Traci M Armand,
Travis E Chapman,
Wanda B Coats
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