FDA Investigator Karen M Cruz Arenas
Karen M Cruz Arenas has conducted inspections on 18 sites in 3 countries as of 20 May 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
18
Last Inspection Date:
20 May 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Korea (Republic of),
Thailand
FDA Investigators that have inspected at least one site in common with Karen M Cruz Arenas:
Adaliz Santaliz Cruz,
Alex M Viehmann,
Althea A Williams,
Amir A Abdalla,
Andrea H Norwood,
Anthony R Bucks,
Barbara T Carmichael,
Bill Tacket, Jr,
Blondell W Johnson,
CDR Sean T Creighton,
Christina L Bigham,
Dawn C Olenjack,
Dianiris C Ayala,
Dolores Harper,
Ebony D Sanon,
Edward E Lockwood (EEL),
Emma R Schaefer,
Eric M Mueller, PharmD,
Eric M Padgett,
Erika V Butler,
Ernest A Clausnitzer,
Frank Wackes,
Georgia A Layloff,
German Rivera,
Gloria J Champagne,
Holly M Scott,
Jacob G Lutz,
James D Planchon,
James I Giefer,
Jason P Aun,
Joey C West,
John C Mcmichael,
Joohi Castelvetere,
Joseph R Strelnik,
Joshua J Silvestri,
Juandria V Williams,
Justin A Boyd,
Kara L Roden,
Karen C Daugherty,
Karen M Rodriguez,
Karthik B Iyer,
Kathleen B Swat,
Kathleen M Bradley,
Kellia N Hicks,
Laiza V Garcia,
Leo J Lagrotte,
Lindsay R Hatch,
Lisa A Warner,
Lydia S Chan,
Margaret A Smithers,
Mary K Concannon,
Matthew H Hunt,
Matthew Ondeck,
Melanie G Warzala,
Michael D Gifford,
Michele L Obert,
Michele Perry Williams,
Monica Cburgos Garcia,
Msdap Gonzlezk,
Nancy G Schmidt,
Patrick L Wisor,
Paul A Licata,
Paula M Laplant,
Phillip M Pontikos,
Richard K Vogel,
Rick L Friedman,
Robert J Ham,
Rohit B Kolhatkar,
Salvatore N Randazzo,
Sandra A Boyd,
Sandra A Hughes,
Shaquenta Y Perkins,
Sherry G Bous,
Shirley J Berryman,
Sidney B Priesmeyer,
Steven D Kehoe,
Thomas J Arista,
Ulysses D Singleton,
Valerie Jgrecek Trinh,
Veronica L Call,
Zachary A Bogorad,
Zedong Dong
Karen M Cruz Arenas's Documents
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