FDA Investigator Donyel M Jones
Donyel M Jones has conducted inspections on 46 sites in 1 countries as of 06 May 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
46
Last Inspection Date:
06 May 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 Donyel M Jones:
Alan D Centi,
Alejandra Mcclellan,
Amber G Chung,
Anastasia M Shields,
Benjamin Bustamante,
Brandon J Brookens,
Brian D Young,
Brian M Brodman,
Craig D Zagata,
Crayton Lee,
Daniel W Johnson,
Denise M Digiulio,
Derek S Dealy,
Devon Jenkins,
Dhaval H Patel,
Diane B Radice,
Donald W Myrick,
Edward D Mcdonald,
Edwin L Hobbs,
Emilio Z Azukwu,
Emmanuel Obulor,
Gayle S Lawson,
Gerald W Kopp,
Giovanni A Vigilante,
Hala L Selby,
James P Mcevoy,
Jeen S Min,
Jesse N Nardone,
Jesse Ray N Nardone,
Jessica M Monteiro,
Jo Annc Declement,
Joseph Brady,
Joseph Duca,
Joseph H Procopio, Jr,
Joseph L Despins, PhD,
Joseph S Fanelli,
Joseph T Dougherty,
Judith A Paterson,
Julianne C Mccullough,
Kelly Doremus,
Kimberly A Coward,
Kristina J Donohue,
Kyle D Covill,
Lawrence R Johnson,
Linda M Hoover,
LTJG Lauren N Shade,
Magdi Ali,
Martha Sullivan Myrick,
Matthew R Noonan,
Maureen A Wentzel,
Michael A Taylor,
Michael L Casner,
Michael Rosner,
Nancy M Lazzari,
Nicholas E Squillante,
Nicholas J Morici,
Nikisha M Bolden,
Peter M Trunk,
Princess R Campbell,
Raffi B Papazian,
Ramanda C Gregory,
Raymond L Cheung,
Rita F Monfort,
Robert C Howard,
Russell P Vandermark,
Sarah K Graham,
Sarah K Lemin,
Seemay A Lee,
Seng Ching Hwang,
Siobhan G Taylor,
Sonia E Ortiz,
Tania E Vizcaino,
Thomas E Friel,
Whitney S Reynolds,
Willy A Orantes,
Xinyi Hui,
Yessika Mashinski
Donyel M Jones's Documents
Publish Date | Document Type | Title |
---|---|---|
June, 2009 | FDA 483 | Penn Herb Company, Ltd. - Form 483, 2009-06-11 |
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