FDA Investigator James L Finn
James L Finn has conducted inspections on 166 sites in 7 countries as of 07 Nov 2003. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
166
Last Inspection Date:
07 Nov 2003
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
Sweden,
United States of America,
Thailand,
Australia,
Canada,
Netherlands,
Indonesia
FDA Investigators that have inspected at least one site in common with James L Finn:
Adam J Taylor,
Alanna L Mussawwir Bias,
Alicia M Mozzachio,
Althea A Williams,
Amanda Dinaro,
Amy M Cramer,
Ann L Demarco,
Audrey Dela Cruz,
Brentley S Collins,
Brett R Havranek,
Brian D Nicholson,
Brian J Davis,
Brian P Emanuel,
Carl A Huffman, III,
Carla A Norris,
Carolyn E Barney,
Catherine J Laufmann,
Charles L Larson,
Chase S Baldwin,
Christi L Bellmore,
Christina A Miller,
Christopher D Leach,
Christopher T Middendorf,
Claire M Minden,
Claudette D Brooks,
Cynthia A Harris, MD, RN,
Daniel J Gorski,
Daniel L Aisen,
Dariusz Galezowski,
David M Amy,
Dawn M Braswell,
Dolores Harper,
Donna K Speer,
Donna Ltartaglino Besone,
Doretha M Tonkins,
Douglas K Avughenbaugh,
Dylan C Grippi,
Elizabeth L Holmes,
Eric S Pittman,
Erin D Mccaffery,
Felix J Marrero,
Fulton A Varner,
Gregory R Dill,
Gregson A Joseph,
Hans T Meyers,
Hassan Ali,
Jacqueline Mdiaz Albertini,
Jacqueline S Warner,
James W Plucinski,
Jamie L Dion,
Janae D Price,
Jason F Chancey,
Jeanne J Chiu,
Jeanne J Thai,
Jennifer A D'angelo,
Jennifer C Adams,
Jennifer C Johnson,
Jesse A Vazquez,
Joan A Loreng,
Jocelyn C Turner,
John A Iwen,
Joseph D Cooper,
Joseph R Haynes,
Joseph R Strelnik,
Joy Rkozlowski Klena,
Justin R Hays,
Kenneth L Smalls,
Kenneth S Boehnen,
Kevin Obrien,
Kimberly Lewandowski Walker,
Kinh Q Mac,
Kip J Hanks,
Kwong P Lee,
Larry F Hallberg,
Latoya A Griffith,
Laurie A Haxel,
Lee Terry Moore,
Lequita M Mayhew,
Logan T Williams,
Margaret Torres Vazquez,
Mark G Peterson,
Mark I Kaspar,
Mary A Millner,
Mei Chiung Huang (Jo),
Michele Gottshall,
Michelle J Glembin,
Misty D Harvey,
Nantie,
Nicholas F Lyons,
Nicole J Clausen,
Nicole S Williams,
Omotunde O Osunsanmi,
Pablo Alcantara,
Paola S Barnett,
Patricia A Cochran,
Patricia A Mcilroy,
Patricia H Dlugosz,
Patrick E Gainer,
Paul M Kawamoto,
Paul W Moy,
Paula P Demichael,
Peterson,
Philip J Boston,
Phung Thien Nguyen,
Prabhu P Raju,
Rafeeq A Habeeb,
Ralph Jerndal,
Rebecca Rodriguez,
Regina T Brown,
Richard L Rutherford,
Robert J Nesselhauf,
Roger J Adams,
Ronald T Weber,
Roshni J Patel,
Russell K Riley,
Shana L Williams,
Shanna R Haden,
Shaquenta Y Perkins,
Sherea L Dillon,
Sinuet P Yashikiramoto,
Stephen D Brown,
Steven P Eastham,
Sullan,
Susan D Yuscius,
Susan O Oladeji,
Tara A Marshall,
Tara C Alcazar,
Thai T Duong,
Todd M Stankewicz,
Tracy K Li,
Truong Xuan Nguyen (Andy),
Uruaku A Obasi,
Vaishali J Patel,
Vlada Matusovsky,
William A Warnick,
William F Lagud, Jr,
William R Weissinger
James L Finn's Documents
Publish Date | Document Type | Title |
---|---|---|
June, 2001 | EIR | BWXT Medical Ltd. - EIR, 2001-06-15 |
February, 2002 | FDA 483 | Sterling Medical Products Intl, Inc. - Form 483, 2002-02-12 |
September, 2002 | EIR | Carriage House Co. Inc., The - EIR, 2002-09-13 |
June, 2000 | EIR | Schwerbrock, Thomas J., DVM - EIR, 2000-06-07 |
September, 2003 | FDA 483 | Hospira, Inc. - Form 483, 2003-09-02 |
June, 2001 | FDA 483 | MDS NORDION - Form 483, 2001-06-15 |
February, 2002 | FDA 483 | M D Technologies, Inc. - Form 483, 2002-02-14 |
September, 2003 | EIR | Hospira, Inc. - EIR, 2003-09-02 |
August, 2002 | EIR | Eversight Illinois, Bloomington - EIR, 2002-08-28 |
October, 2000 | FDA 483 | Labthermics Technologies - Form 483, 2000-10-27 |
August, 2003 | FDA 483 | ENSI-Med Intl. Pty. Ltd. - Form 483, 2003-08-05 |
September, 2003 | FDA 483 Response | Hospira, Inc. - Form 483R, 2003-09-18 |
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