FDA Investigator David J Eide

David J Eide has inspections in 5 countries as of 18 Aug 2023. David J Eide has collaborated with a combinined 3095 experts on various inspections, contributing to compliance and improvement across diverse sectors.

Investigator Details

Number of Inspected Sites:
22
Last Inspection Date:
18 Aug 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America, Italy, China, Mexico
Co-Investigator(s):
Alan E Mehl, Alan L Truong, Albinus M D Sa, Amir Alavi, Ana P Pineda Zavaleta, Andrew A Hoopes, Anthony R Bucks, Ariel Cruz Figueroa, Ashley A Mutawakkil, Barbara L 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 Godeau, 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), 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 Prephete, Guerda Prophete, Gwyn G Dickinson, Hector A Carrero, Helen Y Saccone, Huy T Mai, J Michael Cannon, PhD, Jacqueline Mdiaz Albertine, 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, Jose E Melendez, DDC, Jose R Hernandez, 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, 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, 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 Muniz, 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, Shelby N Marler, Shirley J Berryman, Sidney B Priesmeyer, Simone E Pitts, Sri Ramakrishnaiah Yellela, Srinivas R Chennamaneni, PhD, State Agency, Steven D Dittert, Steven D Kehoe, Steven P Donald, Sumit Sen, Susan M Jackson, Susanna E Ford, Analyst, Tamara J Umscheid, Tara L Breckenridge, Tara L Greene, Tara L King, 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, 2013 FDA 483 Curium US LLC - Form 483, 2013-03-27
March, 2013 EIR Curium US LLC - EIR, 2013-03-27
April, 2009 EIR Hospira, Inc. - EIR, 2009-04-09
January, 2003 EIR TriRx Shawnee LLC - EIR, 2003-01-29
December, 2011 EIR Eurofins BioPharma Product Testing Columbia, Inc. - EIR, 2011-12-16
March, 2004 FDA 483 Ioditech Inc - Form 483, 2004-03-11
April, 2009 FDA 483 Hospira, Inc. - Form 483, 2009-04-09

Experience Redica System's 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

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