FDA Investigator Fe Q Reyes
Fe Q Reyes has inspections in 1 countries as of 02 Nov 2023. Fe Q Reyes has collaborated with a combined 2098 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
62
Last Inspection Date:
02 Nov 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America
Co-Investigator(s):
Aaron J Adler,
Adriana Meza,
Alexandra B Pitkin,
Aliza Chalapong Asawesna,
Ana Djurdjevic,
Andy B Lee,
Angela Shepas,
Anna L Viveros Hernandez,
Anthony E Guzman,
Anthony G Emerson,
Arnold C Shih,
Benigno B Devera,
Bonnie I Needleman,
Bowman,
Brandon R Boone,
Brian E Thompson,
Bush,
Carr Sharpe,
Cathryn M Groehnert,
Celena Ngo,
Cristina E Mosquera,
Darrin E Davis,
David Serrano,
Davis,
Deborah A Greco,
Deborah G Park,
Deborah W Hsu,
Debra A Brown,
Debra C Yamane,
Debra J Fracassa,
Dejon N Harris,
Denise H Howell,
Dennis N Hoang,
Diane R Weidley,
Eileen T Dupont,
Elizabeth M Dahl,
Ellen N Stewart,
Elsa A Kusumoto,
Erik D Sandvig,
Erik M Slama,
Francisco,
Geraldine M Peregrin,
Gordon Chu,
Guillermo,
Hai T Truong,
Henry E Carrillo,
Herminio C Francisco,
Hoover,
James A Barreto,
James P Stallings,
Jeannie Pradyanata,
Jessica B Clark,
Jessica L Andrade,
Jessica L Perkins,
Jinnie Kokiatkulkij,
Joey V Quitania,
John A Liu,
John P Jorgensen,
John R Myung,
Jonathan R Ormond,
Joseph Brady,
Joseph C Francisco,
Joseph C Yen,
Joseph H Lam,
Judy C Nepsa,
Ka L Wong,
Kai Wang,
Katherine E Jacobitz,
Katie T Duong,
Keeshunna D Daniels,
Kevin Lee,
Kevin T Gerrity,
Kham Phommachanh,
Khang K Pham,
Kimberly A Joseph,
Kimberly M Lichter,
Lacresha Menifee,
Laura J Draski,
Lilly O Barton,
Lin Liu,
Ling Yul Liu,
Lourdes M Countee,
Loydis Laureano,
Marco A Solorio,
Mark C Saale,
Mark Gray,
Maurice M Sheehan,
Maxyne T Lam,
Michael F Schuette,
Michael J Chan,
Michael P Dimaano,
Michael S Call,
Natalie J Ayoub,
Natalie J Reese,
Naveen B Walker,
Ngoc T Le,
Nianna C Burns,
Nicholas J Lahey,
Pamela Y Lee,
Patrick R Dimapindan,
Phal K Chhun,
Phillip L Toy,
Rachel E Hauser,
Robert C Hoover,
Rochelle A Rolnik,
Romero,
Ryan J Borges,
Saied A Asbagh,
Sandersk,
Sarah R Barker,
Sean P Desbrow,
Sean P Flood,
Sonya L Karsik,
Sorana Black,
Sunita Vij,
Sylvia A Thomas,
Sylvia R Dooling,
Tamara L Alexander,
Tawny L Colling,
Terrance P Nguyen,
Terry L Boles,
Thao T Kwan,
Tony J Wu,
Tracey T Duong,
Trushani T Desai,
Victoria C Yang,
William J Park,
Yolanda D Mitchell Lee,
Yvette Mlacour Davis,
Yvonne T Lacour
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