FDA Investigator Ellen M Landis
Ellen M Landis has conducted inspections on 89 sites in 2 countries as of 20 Sep 2022. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
89
Last Inspection Date:
20 Sep 2022
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Germany
FDA Investigators that have inspected at least one site in common with Ellen M Landis:
Alexandra P Valencia Guevarez,
Alysia M Salonia,
Alyssa R Favro,
Amanda T Zick,
Amy Wyan Mai,
Andrew F Cohen,
Ann B Okon,
Anne E Carpenter,
Arthur G Hurst,
Ashley Defilippis,
Ashley Polizzotto,
Benton M Ketron,
Bruce G Cooper,
Carley R Anderson,
Carolyn J Cook,
Catherine M Beer,
Dana A Razzano,
Daniel L Aisen,
David A Laplante,
Denise L Terzian,
Diamond M Oden,
Erica B Brush,
Erica B Raphael,
Erin L Nagel,
Gerald T O'connor,
Gerard D Difiore,
Isaac N Baah,
Jackson Y See,
Jacqueline S Warner,
Jamie S Mathews,
Joseph Maselli,
Joseph Milcetic,
Joseph T Frost,
Joshua D Lopez,
Joyce A Williams,
Juan Rjimenez Garcia,
Juanita P Versace,
Judy Keihl,
Jung K Kim,
Kathryn A Nagy,
Kenneth G Klobus,
Kimberly M White,
Kimberly Y Smithson,
Kwong P Lee,
Kyle J Spencer,
LCDR Chad N Thompson,
Lenita R Silvera,
Lirissia Mccoy,
Lisa Mathew,
Margaret E Sarles,
Marie Elena C Puleo,
Mary M Finn,
Meisha A Mandal,
Melissa A Henaghan,
Melissa N Gregorio,
Mercedes G Castillo,
Michael G Sinkevich,
Michael R Dominick,
Mikayla K Deardorff,
Milan S Mcgorty,
Morgan J Matthews,
Nancy A Saxenian Emmons,
Nasser Yazdani, DVM, MPH,
Paul E Stein,
Paul M Gelfand,
Perez,
Peter M Trunk,
Peter R Caparelli,
Randi Lynn Bodoh,
Robert E Moncayo,
Robert J Veitch,
Rupa Pradhan,
Samuel A Francis,
Scott R Izyk,
Shreya Shah,
Slater K Bartlett,
Sonia E Ortiz,
Suwaskie S Smith,
Thomas Siebertz,
Troy R Petrillo,
Wendy A Johnecheck,
Wendy M Stone,
William M Rennells,
William P Chilton,
Yvonne M Santiago
Ellen M Landis's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2017 | FDA 483 | Fieldbrook Foods Corporation - Form 483, 2017-08-11 |
August, 2018 | FDA 483 | DSM-Fermenich - Form 483, 2018-08-16 |
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