FDA Investigator Keishla M Arroyo Lopez
Keishla M Arroyo Lopez has conducted inspections on 41 sites in 2 countries as of 07 Feb 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
41
Last Inspection Date:
07 Feb 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Puerto Rico
FDA Investigators that have inspected at least one site in common with Keishla M Arroyo Lopez:
Abby M Miller,
Alan D Grupe,
Alicia M Weitzel,
Amber M Howell,
Anh Trinh T Nguyen,
Arlene M Badillo,
Avery J Dennis,
Barbara J Rincon,
Beau R Lamb,
Brenda K Alford,
Bruce R Burrell,
Burnsb,
Camille Bennett Hoffman,
Carlos A Medina,
Cathleen A Carr Sharpe,
Ce'nedra M Martin,
Celena Ngo,
Dan C Fisher,
David A Quale,
Devon M Shoop,
Dewey W Darold,
Dirk L Lincoln,
Edward D Harris,
Elizabeth A Sheller,
Elizabeth Q Maccorkell,
Emily M Morrison,
Eric L Scott,
Erica R Mahone,
Frances L Dejesus,
Gordon T Wales,
Harmon M Blanch,
Heika R Tait,
Hugh A Grimoldby,
Ian J Thomson,
Jacob N Hamilton,
James E Trabert,
Jean Brewer,
Jean R Mccurry,
Jeanne M Weishaar,
Jeff A Gard,
Jeff M Uriarte,
Jennifer W Cheng Dobson,
Jessica B Clark,
Jessie J Deloach,
Jinkee Mvila Binayug,
John E Emmert,
Jonathan T Little,
Jorge L Lajara,
Jose F Pedro,
Judy C Nepsa,
Katherine L Arnold,
Katherine V Serrano,
Keegan B Mixon,
Kelsey A Hustedt,
Kelsey A Volkman,
Kevin T Gerrity,
Kimberly Jproctor Jones,
Kristina M Phelps,
Lilly O Barton,
Lisa A Bowden,
Lori J Jennings,
Lourdes Andujar,
LT Rafael Gonzalez,
Lynda L Perry, PhD,
Margo C Jones,
Mark E Imsland,
Matthew R Barr,
Michael J Donovan,
Michael S Call,
Miguel A Martinez Perez,
Mikel T Wright,
Misty L Wallace,
Moraima Jramos Valle,
Nancy E Byerly,
Narahi J Alvarez Alcazar,
Pablo Feliciano,
Rafael Nevarez Nieves,
Rebecca A Sletner,
Rebecca T Davis,
Richard A Martin,
Rocco C Black,
Ronald E Gill,
Sandra K Wangen,
Shahriar Rahmani,
Shelagh D Schopen,
Stanley B Eugene, BS, BME,
Stephanie A Slater, MS,
Steven E Porter, Jr,
Tara A Marshall,
Tara M Pianko,
Thomas C Mclean, CFS,
Timothy D Evans,
Travell D Sawyer,
Xiaojun Yan
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