FDA Investigator David J Eide
David J Eide has conducted inspections on 22 sites in 4 countries as of 16 Feb 2015. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
22
Last Inspection Date:
16 Feb 2015
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Mexico,
China,
Italy
FDA Investigators that have inspected at least one site in common with David J Eide:
Adrienne Morgan,
Alan E Mehl,
Alan L Truong,
Amir Alavi,
Ana P Pineda Zavaleta,
Andrew A Hoopes,
Anthony R Bucks,
Ariel Cruz Figueroa,
Ashley A Mutawakkil,
Barbara I Rogolsky,
Bei Y He,
Bill Tacket, Jr,
Brenda C Hamilton,
Brent M Dehaan,
Brent T Hall,
Brett R Havranek,
Brittany D Terhar,
Bryan S Roddy,
Candace S Tucker,
Carl A Huffman, III,
Carl J Montgomery,
Charles M Edwards,
Chilton L Ng,
Chris A Sack,
Christine A Harman, PhD,
Christopher T Middendorf,
Christopher T Peters,
Cody D Rickman,
Cynthia C Smith, PhD,
Cynthia J Lee, MS,
Cynthia M Goudeau,
Dale A Nyberg,
Damaris Y Hernandez,
Danial S Hutchison,
David A Place,
David M Beltran,
Derrionna M Epps,
Diane L Raccasi,
Donald L Myers,
Dr. Jason R Caballero,
Dustin K Hampton,
Edward E Lockwood (EEL),
Ephrem Hunde, PhD,
Eric C Nielsen,
Eric M Mueller, PharmD,
Eric M Padgett,
Erika V Butler,
Farhana Khan,
Felix Maldonado,
Gayle S Lawson,
Geoffrey K Wong,
Gloria J Champagne,
Gretchen Lf Trendel,
Guerda Prophete,
Gwyn G Dickinson,
Hector A Carrero,
Helen Y Saccone,
Huy T Mai,
J Michael Cannon, PhD,
Jacqueline Mdiaz Albertini,
James I Giefer,
Jamie L Dion,
Janet B Abt,
Jazmine N Still,
Jill J Tillman,
Joan M Nandrea,
John A Iwen,
John A Marchin,
José E Meléndez,
Jose R Hernandez,
Joseph A Piechocki,
Joseph R Lambert,
Julie N Vosilus,
Justin A Boyd,
Karen C Daugherty,
Karen L Kosar,
Karen M Montgomery (KMM),
Katherine Szestypalow,
Kellia N Hicks,
Kelly K Nachtigal,
Ken L Bowers,
Kevin D Kallander,
Kham Phommachanh,
Kristi B Panzer,
Lewis K Antwi,
Linda F Murphy,
Linda R Kuchenthal,
Lisa L Flores,
Lisa L Gilliam,
Logan T Williams,
Lori A Gioia,
Marcus F Yambot,
Margaret A Smithers,
Margaret M Annes,
Maria Estrella,
Marion D Wimberly, Jr,
Matthew H Hunt,
Matthew M Schuckmann,
Matthew R Sleeter,
Matthew Schuckman,
Megan T Ziegler,
Meisha Waters,
Michael C Zubelewicz,
Michele L Obert,
Michele Perry Williams,
Minerva Rogers,
Minh D Phan,
Miranda D Mcdonald,
Monica E Murie,
Monica M Mcclure,
Monique M Brooks,
Nancy G Schmidt,
Neal L Adams,
Nerizza B Guerin,
Noreen Muñiz,
Omotunde O Osunsanmi,
Paige E Shelborne,
Paige E Wilson,
Pamela N Agaba,
Paranthaman Senthamaraikannan,
Patricia L Payne,
Patrick L Wisor,
Paul A Bonneau,
Paula A Trost,
Rafael Nevarez Nieves,
Rafeeq A Habeeb,
Ralph H Vocque,
Randy D Moore,
Regina T Brown,
Rhoda B Eniafe,
Richard L Rutherford,
Rita K Kabaso,
Robert J Ham,
Robin K Reel,
Samina S Khan,
Sandra A Hughes,
Sarah E Rhoades,
Scott A Golladay,
Scott B Laufenberg,
Shafiq S Ahadi,
Sharon K Thoma, PharmD,
Shirley J Berryman,
Sidney B Priesmeyer,
Simone E Pitts,
Sri Ramakrishnaiah Yellela, PhD,
Srinivas R Chennamaneni, PhD,
Steven D Dittert,
Steven D Kehoe,
Steven P Donald,
Sumit Sen,
Susan M Jackson,
Susanna E Ford,
Tamara J Umscheid,
Tara L Breckenridge,
Tara L Greene,
Tara L King,
Tekalign Wondimu,
Thomas J Arista,
Tonya R Johnson,
Tristian E Strait,
Veronica Fuentes, MS,
Vickie J Kanion,
Victoria A Wagoner,
Victoria P Quadrini,
Vikas Moolchandani,
Vlada Matusovsky,
Walden H Lee,
Walsworth,
Warren J Lopicka,
Xiaohan Cai, PhD,
Yiyue Zhang (nmi), PhD,
Zachary A Bogorad,
Zi Qiang Gu
David J Eide's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| March, 2004 | FDA 483 | IodiTech, Inc. - Form 483, 2004-03-11 |
| December, 2011 | EIR | Eurofins BioPharma Product Testing Columbia, Inc. - EIR, 2011-12-16 |
| April, 2009 | EIR | Hospira, Inc. - EIR, 2009-04-09 |
| April, 2009 | FDA 483 | Hospira, Inc. - Form 483, 2009-04-09 |
| January, 2003 | EIR | TriRx Shawnee LLC - EIR, 2003-01-29 |
| March, 2013 | FDA 483 | Curium US LLC - Form 483, 2013-03-27 |
| March, 2013 | EIR | Curium US LLC - EIR, 2013-03-27 |
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