FDA Investigator Jack Ragheb
Jack Ragheb has conducted inspections on 1 sites in 1 countries as of 21 Aug 2019. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
1
Last Inspection Date:
21 Aug 2019
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Jack Ragheb:
Amber G Wardwell,
Andrew M Barlow,
Diane L Raccasi,
Edmund F Mrak, Jr,
Ellen P Madigan,
Haley H Seymour,
Hugh M Mcclure, II,
Jianming Li,
Julie D Bringger,
Kent A Conforti,
LCDR Debra Emerson,
Marilyn Welchenbach,
Megan A Haggerty,
Michelle Yclark Stuart,
Monique C Lo,
Rebecca Rodriguez,
Richard H Penta,
Stephen R Souza,
Susan Kirshner,
Thomas J Arista
Jack Ragheb's Documents
Publish Date | Document Type | Title |
---|---|---|
October, 2008 | FDA 483 | Resilience US, Inc. - Form 483, 2008-10-10 |
October, 2008 | FDA 483 Response | Resilience US, Inc. - Form 483R, 2008-10-31 |
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](https://redica.com/document-store/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