FDA Investigator Tony J Wu
Tony J Wu has conducted inspections on 16 sites in 1 countries as of 10 Jul 2023. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
16
Last Inspection Date:
10 Jul 2023
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 Tony J Wu:
Alexandra B Pitkin,
Ali Hernandez,
Ana Djurdjevic,
Bichsa T Tran,
Bonnie I Needleman,
Brian E Thompson,
Carla J Lundi,
Carrie A Hughes,
Caryn M Everly,
Caryn M Mcnab,
Cassandra L Abellard,
Cathleen A Carr Sharpe,
Cathryn M Groehnert,
Celena Ngo,
Chelsea N Sealey,
Christina D Mello,
Christopher M Elliott,
Darrin E Davis,
David Serrano,
Davis,
Deborah G Park,
Deborah W Hsu,
Dejon N Harris,
Dennis G Poertner,
Desiree C Iya,
Donna Ltartaglino Besone,
Eileen T Dupont,
Fe Q Reyes,
Francisco,
Frederick L Fricke,
Garciam,
Gordon Chu,
Grace P Santos,
Hagstrom,
Jeannie Pradyanata,
Jocelyn E Massey,
Jocelyn E Sparks,
Joe X Phillips,
Joey V Quitania,
John A Gonzalez,
Joseph X Phillips,
Judy C Nepsa,
Julia Ventura,
Ka L Wong,
Kai Wang,
Kaitlyn R Kornberg,
Karen A Wolnik,
Kari M Johansen,
Katherine E Jacobitz,
Kelvin Cheung,
Kelvin X Sanders,
Kim Lthomas Cruse,
Kimberly M Lichter,
Lakecha N Lewis,
Leonard H Lavi,
Lilly O Barton,
Liming Zhang,
Ling Yu L Liu,
Lourdes M Countee,
Marco A Solorio,
Marie Falcone,
Marie T Falcone,
Melanie C Voges,
Michael D Garcia,
Michael S Araneta,
Minh D Phan,
Nicholas J Lahey,
Paquita F Segarra,
Peter C Chow,
Phal K Chhun,
Richard W Tubb,
Richmond K Yip,
Robert C Hoover,
Rochelle A Rolnik,
Saied A Asbagh,
Sara Jdent Acosta,
Sonya L Karsik, RAC,
Steven E Porter, Jr,
Sue Lee Chan,
Susanna N Choi,
Sylvia A Thomas,
Tamala P Magee,
Tanya E Malais,
Tawny L Colling,
Thanh M Andrews,
Timothy P Lafave,
Tracey T Duong,
Tuan D Tran,
Uttaniti Limchumroon (Tom),
Valerie L Whipp,
Virgilio F Pacio, CSO,
Walden H Lee,
Wayne L Jefferson
Tony J Wu's Documents
Publish Date | Document Type | Title |
---|---|---|
September, 2013 | FDA 483 Response | Herbalife Manufacturing, LLC - Form 483R, 2013-10-01 |
September, 2013 | EIR | Herbalife Manufacturing, LLC - EIR, 2013-09-11 |
September, 2013 | FDA 483 | Herbalife Manufacturing, LLC - Form 483, 2013-09-11 |
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