FDA Investigator Jean A Peeples
Jean A Peeples has conducted inspections on 12 sites in 1 countries as of 20 Jun 2014. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
12
Last Inspection Date:
20 Jun 2014
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 Jean A Peeples:
Aaron J Fox,
Angela E Glenn,
Bill Tacket, Jr,
Casey L Hamblin,
CDR Ileana Barreto Pettit,
Cheryl A Clausen,
Christopher J Adams,
Clendening,
Cody D Rickman,
Combs,
Cynthia L Medlin,
Daryl A Dewoskin,
Daudrille K Lowe,
David P King,
David R Heiar,
Denise J Taylor,
Denise M Digiulio,
Dillard H Woody, Jr,
Donald M Mack,
Donna D Gallien, MPH,
Elizabeth D Connell,
Emily E Smith,
Erica M Katherine,
Gerardo Z Vazquez,
Gretchen M Laws,
Howard A Webley,
Hromyak,
Jacquelyn Bradford,
Jennifer L Huntington,
Joanne E King,
Juanelma H Palmer,
Karen G Hirshfield,
Karl D Hezel,
Kenneth R Merritt,
Kimberly J Hoffmeister,
Kimberly L Mcmillan,
Konsuela Y Glass,
Laressa R Gray,
Latorie S Jones,
Laura E Garcia,
Lawrence A Butler,
LCDR Michael H Tollon,
Leo J Lagrotte,
Leslie A Cartmill,
Leslie R Morgan,
Lisa Sg Shelton,
Mabany Lizardi,
Mahaffey,
Marc Balzarini,
Marquis S Allen,
Mcmillan,
Melanie L Drayton,
Mizanne E Lewis,
Nicolas Riveratorres,
Nicole E Knowlton,
Paul L Figarole, Jr,
Ramesh Sood,
Randy N Boling,
Renee J Wilkes,
Robert C Coleman,
Robert E Hultman,
Rodney W Lenger,
Ronald T Weber,
Rose Xu,
Samantha J Pinizzotto, D V M,
Tammara D Perry,
Thomas O Morgan,
Tiana M Mckinley,
Wendy G Tan, PhD,
Zakaria Wahba
Jean A Peeples's Documents
Publish Date | Document Type | Title |
---|---|---|
June, 2000 | EIR | Bausch & Lomb Incorporated - EIR, 2000-06-14 |
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