FDA Investigator Edward Deberry

Edward Deberry has conducted inspections on 308 sites in 4 countries as of 02 Dec 2015. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
308
Last Inspection Date:
02 Dec 2015
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America, Italy, Hungary, Switzerland
FDA Investigators that have inspected at least one site in common with Edward Deberry:
Aaron P Wozniak, Abdur Rashid, Adam R Cooke, Alaric C Denton, Allen F Hall, Alphonso A Haupt, III, Amanda L Evanco, Amy A Johnson, Amy H Ruble, Ana L Kewes, Anastasia M Shields, Ann B Borromeo, April R Bowen, Arlyss M Jones, Arthur G Hurst, Babatunde D Babalola, Betsy C Galliher, Billy M Battles, Bonita S Chester, Brandy D Brown, Brenda Rivera, Brentley S Collins, Brian A Graves, Brittny C Cargo, Burnell M Henry, Carl A Anderson, Carol F Robinson, CDR Thomas R Berry, PPh, Cherrie A Zachary, Cherry R Valerio, Cheryl D Barton, Christopher B May, Christopher J Adams, Christopher S Keating, Claudette D Brooks, Constance Y Fears, Cordelia J Brammer, Crystal A Harlan, Cynthia Jim, CSO, D Ross Spears, PhD, Daphne Santiago, PhD, Darla J Christopher, David E Lowe, David J Leray, David T Glover, David Williams, Davis, Deborah A Greco, Debra J Tucker, Dellarese L Herbert, Demario L Walls, Derek C Price, Devaughn Edwards, Dorothy P Kramer, Douglas L Page, Edecia A Richards, Eileen J Bannerman, Eliezar Ramos, Eric S Weilage, Erika M Wilkerson, Ernest H Blackwood, Esra Toussaint, Fabian Nchaparro Rodriguez, Gabriel R Mclemore, Gamal A Norton, Gary E Coleman, Jr, REHS, Gates E Raynor, Gideon N Esuzor, Hai Lient Phung, Helen R Bester, Hristu B Chepa, Ibad U Khan, Igbinoba, Ivy E Sweeney, Jacqueline Mdiaz Albertini, James P Lewis, Jr, Janet B Gray, Jared P Stevens, Jason F Chancey, Jason K Morgan, Jawaid Hamid, Jeffrey D Sheppard, Jennifer L Bridgewater, Jimmy O Buford, John D Lloyd, John E Aghadia, Johnson, Joseph F Owens, Julie D Bringger, Justin A Boyd, Kemejumaka N Opara, Kenneth L Smalls, Kenny R Robinson, Kimberly Cdelk Brooks, Kip J Hanks, Kunapuli T Madhusudhan, Lareese K Thomas, Larry K Hampton, Laurice Mccoy, Lawrence S Newsom, Lesley K Satterwhite, Leslie W Gilbert, Libia M Lugo, Lillie D Witcher, Mancia R Walker, Marc A Alston, Marcella D Crook, Margaret Torres Vazquez, Marie F Morin, Mark C Saale, Marla A Cassidy, Mary F Bodick, Marybeth Willis, Matthew G Brown, Maya M Davis, Mcbean, Melanie M Walker, Metitia G Sanders, Metitia M Gramby, Miaja Umaedi, Michelle D Haamid, Michelle L Jones, Mihaly S Ligmond, Mokhless A Ghaly, Morrell, Nancy E Fontaine, Nicholas M Smith, Nicole A Lloyd, Nicole D Lyons, Pamela L Velez Vega, Paul A Bonneau, Paula J Bretz, Penny H Mccarver, Perry H Gambrell, Philip Campbell, Prabhu P Raju, R Edwadebey Deberry, Rachael L Cook, Radona R Boutte, Randy L Clarida, Rashard A Knight, Rashonda N Rucker, Rebecca Rodriguez, Richard J Bashay, Richard L Garcia, Robert C Coleman, Robert D Tollefsen, Robert J Rutherford, Robert Q Green, Robert W Turner, Robin N Goins, Russell K Riley, Sally Gopaul, Sandra I Gaul, Sandra R Saunders, Scott T Ballard, Seneca D Toms, Sereen Gmorgan Murray, Shayla G Turnipseed, Shusheen A Alexander, Simone M Edmonson, Siobhan G Taylor, Sonya M Edmonds, Stanley Nelson, Jr, Stephanie E Hubbard, Stephanie L Kelly, Stephen D Brown, Steven M Weinman, Susan M Taylor, Susan T Hadman, Tamara M Casselman, Tammara A Newberry, Tammara A Stephens, Theresa L Stewart, Timothy T Kapsala, Tomika L Bivens, Tracy L Ramseur, Tracy R Ball, Tyrico K English, Vanessa E Coulter, Veronica Fuentes, MS, Vicky C Stoakes, Victoria L Palmer, Vincent M Williams, Viviana Matta, Weedb, William P Tonkins, Young Kim

Edward Deberry's Documents

Publish Date Document Type Title
September, 2008 FDA 483 King Bio Inc - Form 483, 2008-09-25
September, 2007 EIR Baxter Healthcare Corporation - EIR, 2007-09-19
September, 2008 EIR Greer Laboratories, Inc. - EIR, 2008-09-15
September, 2015 FDA 483 King Bio Inc - Form 483, 2015-09-04
September, 2006 EIR Greer Laboratories, Inc. - EIR, 2006-09-18
September, 2012 EIR Nypro Inc. - EIR, 2012-09-12
September, 2009 EIR Nypro Inc. - EIR, 2009-09-09
June, 2010 EIR Greer Laboratories, Inc. - EIR, 2010-06-29

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.

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