FDA Investigator Kris K Moore
Kris K Moore has conducted inspections on 113 sites in 1 countries as of 03 Jun 2004. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
113
Last Inspection Date:
03 Jun 2004
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 Kris K Moore:
Albert M Brindle,
Annemarie Bodnar,
Antoinette L Ravelli,
Austin B Appler,
Brian D Young,
Carol A Perry,
Carol A Robles,
Cary Greene,
Charles J Chacko,
Craig W Swanson,
Derek S Dealy,
Devon Jenkins,
Dhaval H Patel,
Edward O'shaughnessy,
Gianine E Delade,
Gianine E Tompkins,
Jason M Sluzynski,
Jessica M Monteiro,
Jill M Sooter,
Jill Mielziner,
Jo Annc Declement,
Joseph T Dougherty,
Judith A Jones,
Judith A Paterson,
Justine Tomasso,
Karen F Tomaziefski,
Keith A Schwartz,
Kelli F Dobilas,
Kelly Doremus,
Kerry A Kurdilla,
Kyle S Hobson,
Laishan L Lam,
Lawrence R Johnson,
Loretta Nemchik,
Marcelo O Mangalindan, Jr,
Melissa B Libby,
Meredith L Sheridan,
Michael Rosner,
Ramanda C Gregory,
Ray Niles,
Raymond L Cheung,
Raymond Niles,
Remache,
Ruth A Oni,
Schultz,
Schwartz,
Seng Ching Hwang,
Sherri J Liu,
Susan M Halsted,
Teigan M Mule,
Tressa T Lewis,
Valerie C Reed,
William J Muszynski,
William W Dotts,
Yessika Mashinski
Kris K Moore's Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2000 | FDA 483 Response | Delaware River & Bay Authority Cape May-Lewes Ferry - Form 483R, 2000-07-17 |
July, 2000 | EIR | Delaware River & Bay Authority Cape May-Lewes Ferry - EIR, 2000-07-12 |
June, 2000 | EIR | Delaware River & Bay Authority Cape May-Lewes Ferry - EIR, 2000-06-14 |
July, 2000 | FDA 483 | Delaware River & Bay Authority Cape May-Lewes Ferry - Form 483, 2000-07-12 |
June, 2000 | FDA 483 | Delaware River & Bay Authority Cape May-Lewes Ferry - Form 483, 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