FDA Investigator Ann B Borromeo

Ann B Borromeo has conducted inspections on 470 sites in 1 countries as of 03 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
470
Last Inspection Date:
03 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
100008649
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Ann B Borromeo:
Abby Lmozeke Baker, Adam R Cooke, Amanda M Osteen, Ana C Lazo, Angela G Wagley, Anna E Fain, Barbara D Wright, Barbara M Frazier, Benjamin E Bowen, Benjamin P Stewart, Bernardica T Sculac Stern, Bonita S Chester, Bonnie E Conley, Bonnie E Pierson, Brandon C Heitmeier, Brandy D Brown, Brian S Lynch, Caitlin L Almonrode, Carl A Huffman, III, Charvais S Hill, Cherie T Parker, Cheryl A Grandinetti, Cheryl G Scott, Cheryl L Watson, Christopher J Adams, Christopher M Jeffers, Christopher S Keating, Claire M Minden, Clendening, Clinton J Lott, Cody D Rickman, Combs, Constance Y Fears, Cynthia L Medlin, Dana M Klimavicz, Daniel L Aisen, Danielle M Maddox, David R Heiar, David Williams, Dawn C Olenjack, Deborah A Greco, Decima L Thompson, Decima L Washington, Delisa R Davis, Demario L Walls, Donna D Gallien, MPH, Dorothy P Kramer, Dr. Koffi A Amegadje, Edward Deberry, Edward H Maticka, Eileen J Bannerman, Elizabeth D Connell, Emily A Baldwin, Emily A Green, Eric R Holm, Fabian Nchaparro Rodriguez, Francis A Guidry, Frank Flores, Gail L Katz, George J Flynn, Gretchen M Laws, Harry J Brewer, Henry E Sanchez, Holly M Scott, Ibad U Khan, Inga M Warr, Iram R Hassan, PhD, Jamie P Webb, Jannet M Peroti, Jared P Stevens, Jason D Abel, Jason K Morgan, Jawaid Hamid, Jeff Kirksey, Jennifer M Heitz, Joanne E King, John E Russell, Jr, Johnathan M Crayton, Joseph F Owens, June P Page, Justin N Henson, Karen Gale Sego, Kari L Batey, Kathleen B Swat, Katrina B Mosley Sloan, Kellie R Riggs, Kenneth R Merritt, Kerry Ann Latham, Kimberly A Dutzek, Kimberly L Mcmillan, Kip J Hanks, Konsuela Y Glass, Krista W Whitten, Lacey J Chessor, Lareese K Thomas, Larry K Hampton, Laura L Staples, LCDR Angelica M Chica, LCDR Matthew R Mcnew, MPH, REHS/RS, Leon L Crawley, Linda A Gregory Duty, Lindsay H Bertling, Llopis, LTJG Lauren N Shade, Mahaffey, Margaret E Slimbach, Marie F Morin, Marshall A Naimo, Marshall H Kinsey, Martrice A Packer, Marvin D Jones, Matthew R Coleman, Mcmillan, Melanie L Drayton, Meocha V Whaley, Myla D Chapman, Natalie A Guidry, Natasha N Mccants, Nicole M Bell, Osama A Khatib, Pamela M Thomas, Patricia S Smith, Patrick C Dooley, Peggy A Stogner, Penny H Mccarver, Randy L Clarida, Richard J Bashay, Robert E Hultman, Ronnie E Jackson, Samantha E Cleek, Samantha J Bradley, Sereen Gmorgan Murray, Shondra N Gipson, Sonya M Edmonds, Stephanie E Hubbard, Stephanie Mangigian, MS/OSH, RN, Stephen G Mclane, Steven D Banks, Steven D Dittert, Susan O Oladeji, Takiyah S Gilmore Embery, Thomas B Smith, Timothy H Vo, Traci M Armand, Tracy R Ball, Trang N Cox, Travis E Chapman, Vanessa E Coulter, Veronica Fuentes, MS, Victor Spanioli, Viviana Matta, Wendy R Blame, Whitney M White, Zachary J Conlin, Zada L Giles

Ann B Borromeo's Documents

Publish Date Document Type Title
September, 2002 EIR DCI Donor Services dba Tennessee Donor Services (Tri-Cities) - EIR, 2002-09-23
March, 2024 FDA 483 Louisiana State University (school Of Veterinary Medicine) - Form 483, 2024-03-14
June, 2013 EIR Richard K. McDavid, MD - EIR, 2013-06-20
May, 2018 FDA 483 Martin G. Pomper, MD - Form 483, 2018-05-25
May, 2012 EIR East Tennessee Clinical Research, Inc - EIR, 2012-05-29
September, 2002 FDA 483 Response Blood Assurance Inc. - Form 483R, 2002-09-18
September, 2003 FDA 483 Biomat USA, Inc. - Form 483, 2003-09-11
June, 2013 FDA 483 Richard K. McDavid, MD - Form 483, 2013-06-20
March, 2011 FDA 483 PETNET SOLUTIONS, INC. - Form 483, 2011-03-10
December, 2004 FDA 483 Labs Inc Labs - Form 483, 2004-12-17
April, 2015 FDA 483 Vanderbilt University Medical Center RDRC - Form 483, 2015-04-01
May, 2023 FDA 483 East Tennessee Clinical Research, Inc - Form 483, 2023-05-26
September, 2001 EIR Custom Foods of Americ Inc. - EIR, 2001-09-05
August, 2016 EIR William E. Kirby, MD - EIR, 2016-08-04
February, 2021 EIR Craig R Reinemeyer, DVM PhD - EIR, 2021-02-16
November, 2011 FDA 483 National Embryo Donation Center - Form 483, 2011-11-10
September, 2002 FDA 483 Blood Assurance Inc. - Form 483, 2002-09-12
October, 2023 FDA 483 Sebela Women's Health Inc. - Form 483, 2023-10-13
December, 2022 FDA 483 Melanie M Hoppers, MD - Form 483, 2022-12-15
November, 2020 FDA 483 Paul A. Goepfert, MD. - Form 483, 2020-11-20
October, 2019 FDA 483 Jan L. Brandes, M.D. - Form 483, 2019-10-18
January, 2019 FDA 483 William E. Kirby, MD - Form 483, 2019-01-17
July, 2000 EIR Pharma Packaging Solutions, LLC dba Tjoapack, LLC - EIR, 2000-07-12
March, 2021 EIR John P Devincenzo MD - EIR, 2021-03-16
June, 2017 FDA 483 Jitrenda Gandhi - Form 483, 2017-06-01
August, 2002 EIR East Tennessee Lions Eye Bank - EIR, 2002-08-29
August, 2023 FDA 483 Angela D. Ritter, M.D. - Form 483, 2023-08-17
October, 2014 EIR East Tennessee Clinical Research, Inc - EIR, 2014-10-21
January, 2000 FDA 483 DRS Returns, Llc. - Form 483, 2000-01-03
September, 2018 FDA 483 Ashwani K. Singal, M.D. - Form 483, 2018-09-28
January, 2000 EIR DRS Returns, Llc. - EIR, 2000-01-03
May, 2023 EIR East Tennessee Clinical Research, Inc - EIR, 2023-06-14
April, 2024 FDA 483 Han C. Phan, M.D. - Form 483, 2024-04-05

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