FDA Investigator Tony T Yang
Tony T Yang has conducted inspections on 190 sites in 10 countries as of 21 Dec 2010. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
190
Last Inspection Date:
21 Dec 2010
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
China,
Mexico,
Korea (Republic of),
Japan,
Poland,
Malaysia,
Philippines,
Taiwan,
Thailand
FDA Investigators that have inspected at least one site in common with Tony T Yang:
Aaron L Dunbar,
Adaliz Santaliz Cruz,
Aimee J Edwin,
Albert L Nguyen,
Alison A Nicoli,
Alison A Stone,
Althea A Williams,
Amy L Mcintyre,
Amy M Cramer,
Ana M Placencia,
Annabelle Crusan, D,VM,
Anthony L Nicoli,
April L Young,
Arthur G Hurst,
Ashley A Segura,
Benjamin J Dastoli,
Benjamin W Anderson,
Billi Jom Johnson,
Brian D Nicholson,
Brian R Hendricks,
Byungja E Marciante,
Calvin K Cook,
Carolyn A Warren,
Catherine J Laufmann,
Charles I Ann,
Charles L Larson,
Charles R Cote, RIC,
Christina L Bigham,
Clifford F Long,
Courtney R Ingalsbe,
Cynthia A Harris, MD, RN,
Daniel J Lahar,
Daniel L Aisen,
Darren D Holaday,
Debra L Curtis,
Demetria L Lueneburg,
Denise L Burosh,
Diane T Reindl,
Dianiris C Ayala,
Dipesh K Shah,
Dolores Harper,
Douglas W Atkins,
Edward A Fabiano,
Elizabeth P Mayer,
Ellen C Weisensel,
Eric M Padgett,
Evelyn Taha,
Fannie M Harrell,
Frank J Marciniak,
Grant M Ruis,
Gregory W Smith,
Gregson A Joseph,
Heather Akleimola Hulbert,
Howard A Burmester,
Ivan E Reyes,
Jaclyn N Munsch,
James A Beaulieu,
James K Ireland,
James W Leonette,
Janete F Guardia,
Janis R Armedoriz,
Jasjeet K Sekhon,
Jay V Jariwala,
Jennifer S Ness,
Jeremy L Tri,
Jessica L Johnson,
Jessica M Novak,
Jocelyn M Muggli,
John E Emmert,
Joseph D Gong,
Joseph M Edwin,
Joshua J Silvestri,
Justin A Hefferman,
Karen M Labounty,
Karla J Youngberg,
Katherine A Clarke Girolamo,
Kellie L Thommes, RN,
Kellie L Westerbuhr,
Kelvin Cheung,
Kenneth A Libertoski,
Kibily D Dembele,
Kimberly Lewandowski Walker,
Kirtida Patel,
Kyle J Mccracken,
Larae M Koopman,
Leo J Lagrotte,
Leonard H Lavi,
Leonardm,
Linda V Weyer,
Lori B Wikstrom,
Lori S Lawless,
Maria E Treadwell,
Marie A Fadden,
Marissa S Henning,
Marissa S Steinhagen,
Mei Chen Mu,
Melinda L Rice,
Melissa I Michurski,
Miaja Umaedi,
Michael K Larson,
Michelle J Glembin,
Mildred J Tures,
Miles D Foster,
Minh D Phan,
Mohammed H Adam,
Msdap Gonzlezk,
Nicole C Victoria, PhD,
Nikki S Bryant,
Norman Wong,
Nydia E Colon,
Paola E Lathrop,
Patrick J Campbell,
Perry H Gambrell,
Peter T Erlandson,
Ralph Jerndal,
Rebecca L Caulfield,
Rhonda L Mecl,
Richard Jay Tucker, RS,
Richard K Vogel,
Robert H Claflin,
Robert J Waldorf,
Ryan J Benedict,
Sarah A Hassas,
Sarah A Palmer,
Scott B Laufenberg,
Shafiq S Ahadi,
Sharon L Matson,
Sharon M Harold,
Shaun M Olson,
Sonya L Karsik, RAC,
Stephen D Eich,
Steven J Crowston,
Steven R Ziser,
Susan A Atcher,
Susan M Atcher,
Susan M Matthias,
Tara C Singh,
Thai T Duong,
Theresa C Klaman,
Timothy G Philips,
Timothy R Marrs,
Traci C Kelm,
Tracy A Solseng,
Troy A Brenny,
Tyler R Courtney,
Tyson J Eldridge Stedman,
Vivian Garcia,
Wayne W Grundstrom,
Wendy R Blame,
William D Tingley,
William E Keer,
Yehualashet A Gessesse,
Zachary P Wachlarowicz
Tony T Yang's Documents
Publish Date | Document Type | Title |
---|---|---|
January, 2001 | EIR | Scimed Life Systems,Inc - EIR, 2001-01-09 |
January, 2000 | FDA 483 | Boston Scientific Corporation - Form 483, 2000-01-14 |
August, 2001 | EIR | Asahi Kasei Medical MT Corp. Oita Works - EIR, 2001-08-10 |
June, 2010 | FDA 483 | Dane Technologies - Form 483, 2010-06-17 |
October, 2000 | FDA 483 | Electromed, Inc. - Form 483, 2000-10-16 |
November, 2010 | FDA 483 | Apex Medical Corporation - Form 483, 2010-11-17 |
March, 2002 | FDA 483 | Gyrus ACMI Inc. - Form 483, 2002-03-04 |
July, 2003 | FDA 483 | Micromedics, Inc. - Form 483, 2003-07-29 |
August, 2001 | FDA 483 Response | Asahi Kasei Medical MT Corp. Oita Works - Form 483R, 2001-09-07 |
November, 2003 | EIR | Sunder Biomedical Tech Co., Ltd. - EIR, 2003-11-14 |
November, 2003 | FDA 483 | Sunder Biomedical Tech Co., Ltd. - Form 483, 2003-11-14 |
July, 2001 | FDA 483 | Radiation Products Design,Inc - Form 483, 2001-07-24 |
April, 2000 | EIR | Boston Scientific Corporation - EIR, 2000-04-07 |
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.
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