FDA Investigator Jennifer L Sheehan

Jennifer L Sheehan has conducted inspections on 233 sites in 3 countries as of 02 Jul 2024. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
233
Last Inspection Date:
02 Jul 2024
Investigator Role:
FDA Investigator
Redica ID:
100002502
Countries of Inspections:
United States of America, Germany, Canada
FDA Investigators that have inspected at least one site in common with Jennifer L Sheehan:
Alan Escalona, Alanna L Mussawwir Bias, Alexander M Kay, Allison C Hunter, Allison E Sincek, Allison M Scheck, Amy A Johnson, Andrea D Swingle, Andrew I Carr, Andrew M Kupper, Andria L Kuhlman, Anissa C Kelley, Anna M Brannen, Arie R Dyk, Arindam Dasgupta, PhD, Bailey A Uetrecht, Barbara A Rusin, Barbara G Peoples, Barbara M Frazier, Benjamin D Shuler, Bonita S Chester, Brandon L Mariner, Brenda C Hamilton, Brigitte K Hofmann, Bryan J Love, Carl E Lovrich, Carla J Lundi, Cassandra L Winters, CDR Kimberly Y Martin, Christian L Witkovskie, Christina L Bigham, Christine E Kelley, Christopher J Adams, Christopher T Middendorf, Claire M Minden, Craig A Garmendia, Craig P Seaborn, Craig T Rybus, Cynthia A Harris, MD, RN, Cynthia L Rakestraw, D'arbra R Blankenship, David P Moorhead, Diane Hall, Donna F Campbell, Doretha M Tonkins, Erica L Nicoll, Genevieve E Ghand, Geoffrey K Kilili, George C Amedro, George J Flynn, Gerald Mierle, Geraldine D Sanders, Guy W Cartwright, Helen B Ricalde, Holly J Wilson, Hugh M Mcclure, II, Ifueko Osemwota, Jaime E Perry, James G Marsh, James W Leonette, Jamie L Johnson, Jason D Werne, Javonica F Penn, Jazmine N Still, Jennifer L Jager, Jennifer M Heitz, John A Kadavil, PhD, John D Jaworski, John E Russell, Jr, Jonah S Ufferfilge, Jonathan A Ferguson, Joseph X Kaufman, Joshua S Hunt, Judy Ellen Ciaraldi, Karen M Cooper, Karen M Kondas, Katherine Szestypalow, Kathryn Suttling, Kellie R Riggs, Kelly D Moore, Kenneth E Felkley, Kenneth L Smalls, Laressa R Gray, Larry K Austin, Laura E Garcia, Laureen F Kononen, Laureen M Geniusz, Lauren M Lilly, PhD, Lauren N Smith, Lauren R Collins, Lawrence Y Lee, PhD, LCDR Wilfred A Darang, Leena Thomas, Leigh Anne Myers, Leslie W Gilbert, Li Hongpaul Yeh, PhD, Linda S Mattingly, Lindsey M Schwierjohann, Lisa P Oakes, Luckner Jean Marie, Maney P Sturgill, Marcia A Worley, Marianne Allen, Maribeth G Niesen, Marion W Nadeau, Martin K Yau, PhD, Mary B Sheets, Mary R Kirker, Mary T Carden, Matt D Suedkamp, Matthew B Casale, Matthew J Gretkierewicz, Melkamu Getie Kebtie, PhD, Michael I Gorman, Michael J Schibi, Nadeem I Chaudhry, Nancy A Bellamy, Nancy L Meade, Nancy L Neiger, Nicola M Fenty Stewart, Nisha C Patel, Patrick D Stone, MS, Paula J Bretz, Paula M Laplant, Philip S Woodward, Phillip M Pontikos, Pifer, Richard J Bashay, Richard W Berning, Robert L Lewis, Jr, Robert W Hudson, Rosanna M Goodrich, Roy C Stephens, Samantha J Pinizzotto, D V M, Sean R Moynihan, MPH, Seongeun Cho (Julia), PhD, Shannon A Gregory, Sherry L Secrist, BLT DO, Sripal R Mada, PhD, Stephen J Kilker, Stephen J Rabe, Steven D Banks, Susan D Yuscius, Susan M Taylor, Teresa K Kastner, Thomas B Smith, Thomas J Prigge, Thomas W Nojek, Thunder N Dunkijacobs, Travis R Hunt, Troy A Huffman, Vickie J Kanion, William D Bassett, Jr, Yvette Mlacour Davis

Jennifer L Sheehan's Documents

Publish Date Document Type Title
September, 2019 EIR Hoxworth Blood Center University of Cincinnati - EIR, 2019-09-04
April, 2021 FDA 483 Louisville Reproductive Center - Form 483, 2021-04-13
July, 2014 FDA 483 Dixie Dew Products Inc - Form 483, 2014-07-10
March, 2022 EIR The Christ Hospital Health Network - EIR, 2022-03-15
March, 2023 FDA 483 Bethesda Fertility Center - Form 483, 2023-03-22
April, 2013 EIR David J. Portman M.D. - EIR, 2013-04-11
November, 2021 FDA 483 Predictable Surgical Technologies - Form 483, 2021-11-18
October, 2014 FDA 483 Manisha H Shah, M.D. - Form 483, 2014-10-17
August, 2021 FDA 483 CSL Plasma Inc - Form 483, 2021-08-11
April, 2013 EIR David J. Portman M.D. - EIR, 2012-10-26
August, 2023 FDA 483 Institute for Reproductive Health - Form 483, 2023-08-30
July, 2021 FDA 483 Institute for Reproductive Health - Form 483, 2021-07-14
February, 2020 FDA 483 Biomat USA, Inc - Form 483, 2020-02-11
August, 2022 FDA 483 RenatiLabs Inc - Form 483, 2022-08-12
October, 2014 EIR Manisha H Shah, M.D. - EIR, 2014-10-17
August, 2021 FDA 483 SpringCreek Fertility - Form 483, 2021-08-02
March, 2016 EIR Saint Elizabeth Med Ctr IRB - EIR, 2016-03-09
November, 2023 FDA 483 Predictable Surgical Technologies - Form 483, 2023-11-08
March, 2022 FDA 483 Department of Air Force 88th Medical Group SGQC WPAFB - Form 483, 2022-03-30
February, 2014 EIR Michael J Noss MD - EIR, 2014-02-20
June, 2017 FDA 483 Louisville Reproductive Center - Form 483, 2017-06-15
January, 2024 FDA 483 Octapharma Plasma Inc - Form 483, 2024-01-10
June, 2014 EIR LifeNet Health - EIR, 2014-06-09
March, 2019 FDA 483 Bio-Blood Components Inc - Form 483, 2019-03-07
December, 2021 FDA 483 Center for Fertility and Reproductive Endocrinology UPP - Form 483, 2021-12-08
September, 2019 FDA 483 Hoxworth Blood Center University of Cincinnati - Form 483, 2019-09-04
March, 2015 EIR Bernadette D'Souza, MD - EIR, 2015-03-18
April, 2013 FDA 483 David J. Portman M.D. - Form 483, 2012-10-26
April, 2024 FDA 483 Alpha Orthopedic Systems, LLC - Form 483, 2024-04-29
September, 2023 FDA 483 Kentucky Blood Center Inc - Form 483, 2023-09-18
June, 2017 EIR Louisville Reproductive Center - EIR, 2017-06-15
July, 2019 FDA 483 CSL Plasma Inc - Form 483, 2019-07-18
September, 2019 FDA 483 Department of Air Force 88th Medical Group SGQC WPAFB - Form 483, 2019-09-26

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