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.
![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