FDA Investigator Wr Bowman
Wr Bowman has conducted inspections on 63 sites in 3 countries as of 09 May 2011. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
63
Last Inspection Date:
09 May 2011
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America,
India,
Canada
FDA Investigators that have inspected at least one site in common with Wr Bowman:
Alan M Stevens,
Alexandra B Pitkin,
Allen F Hall,
Althea A Williams,
Amanda E Lewin, PhD,
Anderson,
Bailey A Uetrecht,
Barbara A Rusin,
Barbara M Frazier,
Bruce R Burrell,
Bush,
Carol B Czerniak,
Cathleen A Carr Sharpe,
Cathryn M Groehnert,
CDR Sean T Creighton,
Celena Ngo,
Charles L Larson,
Cheron M Portee,
Christine I Shaw,
Christopher M Elliott,
Corey A Cruse,
Courtney N Long,
Dannie E Rowland,
Darrin E Davis,
David G Whitman,
David Kalins,
Davis,
Debra D Devlieger,
Debra J Fracassa,
Desiree C Iya,
Diana M Rand,
Dolores Harper,
Donna Ltartaglino Besone,
Dr. Sriram Subramaniam, PhD,
Durell L Giles,
Eileen T Dupont,
Elizabeth A Dakan,
Elizabeth M Dahl,
Erik D Sandvig,
Finn A Slizza,
Francisco,
Garciam,
Gene D Arcy,
Geoffrey K Kilili,
Greg K Keshishyan,
Gulshan R Anand,
Hagstrom,
Henry E Carrillo,
Herminio C Francisco,
Hyojong Kwon, PhD,
Ian A Pilcher,
Iris C Macinnes,
Ivar J Sohn,
Jake T Lane,
James A Barreto,
James R Fleckenstein,
Jamie M Du,
Janet Pulver,
Jeffrey P Raimondi,
Jinnie Kokiatkulkij,
Jocelyn E Massey,
Jocelyn E Sparks,
Joey V Quitania,
John A Kadavil, PhD,
John R Myung,
Joseph H Lam,
Juanj N Wu,
Judy C Nepsa,
Ka L Wong,
Kai Wang,
Katherine E Jacobitz,
Kelvin Cheung,
Kelvin X Sanders,
Kip J Hanks,
Kirtida Patel,
Lakecha N Lewis,
Laurissa S Flowers,
Leonard H Lavi,
Li Hongpaul Yeh, PhD,
Lilly O Barton,
Linda Galindo,
Linda Linh N Adams,
Linda R Kuchenthal,
Lori A Gioia,
Mageet,
Marc G Bellaire,
Marcus F Yambot,
Maria Isabe Tejero Del Rio,
Mark C Saale,
Mark W Babbitt,
Marlo Ianm Alintanahin,
Matthew C Kristof,
Matthew J Gretkierewicz,
Matthew M Vernon,
Maurice M Sheehan,
Mei Chen Mu,
Michael P Dimaano,
Michael S Call,
Natalie J Ayoub,
Nianna C Burns,
Nicholas J Lahey,
Rebecca T Davis,
Richard W Tubb,
Robert C Hoover,
Rodney T Allnutt,
Ruben C Ayala, PharmD,
Sarah A Hassas,
Scott B Laufenberg,
Scott K Zika,
Sean P Desbrow,
Selene T Torres,
Shaquenta Y Perkins,
Sonya L Karsik, RAC,
Stacie A Woods,
Stephen R Souza,
Sundy V Sedwick,
Sunita Vij,
Taichun Qin, PhD,
Tamala P Bogan,
Tamala P Magee,
Tamara L Alexander,
Tanya E Malais,
Tawny L Colling,
Thanh M Andrews,
Thao T Kwan,
Truong Xuan Nguyen (Andy),
Trushani T Desai,
Uttaniti Limchumroon (Tom),
Vickie L Anderson,
Victor H Loo,
Virgilio F Pacio, CSO,
Youkeun Kim,
Yumi J Hiramine,
Yvette E Guillermo,
Zachary A Bogorad
Wr Bowman's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| October, 2001 | FDA 483 | Bio Science Technologies Inc - Form 483, 2001-10-29 |
| June, 2004 | EIR | Medtronic MiniMed, Inc. - EIR, 2007-12-21 |
| February, 2000 | FDA 483 | Limberg Eye Center - Form 483, 2000-02-14 |
| September, 2008 | FDA 483 | ACCUTEST RESEARCH LABORATORIES ( I ) - Form 483, 2008-09-01 |
| April, 2001 | FDA 483 | CareFusion 303, Inc. - Form 483, 2001-04-12 |
| November, 2002 | FDA 483 | The Belport Company, Inc DBA Gingi-Pak - Form 483, 2002-11-14 |
| January, 2000 | FDA 483 | Medtronic MiniMed - Form 483, 2000-01-10 |
| April, 2001 | EIR | CareFusion 303, Inc. - EIR, 2001-04-12 |
| February, 2000 | EIR | Michael B. Limberg - EIR, 2000-02-14 |
| September, 2008 | EIR | ACCUTEST RESEARCH LABORATORIES ( I ) - EIR, 2008-10-16 |
| April, 2002 | EIR | Allergan - EIR, 2002-04-05 |
| October, 2001 | EIR | Bio Science Technologies Inc - EIR, 2001-10-29 |
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