FDA Investigator La Tasham Gunter

La Tasham Gunter has conducted inspections on 183 sites in 4 countries as of 01 Jul 2024. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
183
Last Inspection Date:
01 Jul 2024
Investigator Role:
FDA Investigator
Redica ID:
100008551
Countries of Inspections:
United States of America, Italy, Japan, Spain
FDA Investigators that have inspected at least one site in common with La Tasham Gunter:
Adriana N Jimenez Lopez, Alice C Silva, Amanda B Athey, Amanda B Vega, Amanda M Osteen, Amber G Chung, Amy A Johnson, Amy C Amaro, Amy Malla, Ana P Barido, Andrea S Heise, Andrew A Leboeuf, Andrew J Gonzales, Ashley M Whitehurst, Austin B Appler, Barbara A Burke, Barbara A Gullick, Barbara D Wright, Barbara G Peoples, Barbara J Holladay, Brandon L Mariner, Brian M Palermo, Brooke K Higgins, Bryan J Love, Carrie L Doupnik, Chaltu Nwakijra, Charlean R Butler, Charles D Boison, Charles M Kerns, BLT DO, Christopher D Leach, Collins M Mason, Conrad M Guardia, Courtney N Long, Danielle R Rainey, David K Glasgow, David L Chon, David P Rice, Jr, Dawn M Collins, Dennis L Doupnik, Dennis R Hudson, Diane Hall, Donna D Gallien, MPH, Earl Echon, Edette J Newby, Elvis D Morton, Emest F Bizjak, Esaw, Esther A Ofori, Gail L Katz, Gale L Glinecki, Garry H Stewart, Gerald D Bromley, Jr, Gerald Mierle, Gifford Whitehurst, Jr, Heath R Harley, Holly S Simms, James M Simpson, James T Mccoy, Jamie D Richardson, Jamie D Swann, Jennifer A Jones, Joey C West, John Dan, John J Thibodeau, John M Gusto, Johnson, Jonathan W Chapman, Joseph W Matthews, Joyce B Watson, Judy Ellen Ciaraldi, Justin A Hefferman, Karen M Cooper, Kellie L Westerbuhr, Kenneth L Smalls, Kenneth Nieves, Kent A Conforti, Kimberley A Hoefen, Kip J Hanks, Lakisha M Williams, Laurianne M Montonye, Laurie A Haxel, Laurissa S Flowers, LCDR Anastasia M Piliafas Brown, LCDR Matthew R Mcnew, MPH, REHS/RS, LCDR Wilfred A Darang, Leena Thomas, Linda J Eason, Linda S Mattingly, Lorayne A Mcguinness, LT John M Mastalski, LT Melanie M Mayor, USPHS, Lucas B Leake, Luis A Carrion, Marcus A Ray, Margaret H Waters, Margaret Torres Vazquez, Marie B Buen Bigornia, Marilyn M White, Marion W Nadeau, Marlene L Davis, Mary T Carden, Melissa D Kalik, Michael S Call, Mildred L Mccray, Nancy L Meade, Nebil A Oumer, Nina D Patel, Nisha C Patel, Norman Fogg, Oumou Barry, Patricia A Morrow, Patrick C Klotzbuecher, Paula J Bretz, Pelekakis, Pratik S Upadhyay, DDC, Regina Gibson Melton, Renisha M Shaw, Richard J Bashay, Rina Bhikha, Ronald T Nowalk, Sandra Sejdinovic, Sarah Forney, Sarah J Park, Sean R Moynihan, MPH, Shavon L Square, Sherry L Secrist, BLT DO, Sherry M Nisson, Shusheen A Alexander, Stacey A Priest, Stephany J Wesley, Stephen C Eason, Susan J Essenmacher, Susan M Miller, Tajah L Blackburn, Tamara N Champion, Tamika E Allen, RN, Tania E Vizcaino, Thomas J Hudson, Thomas W Nojek, Tiki J Dixon, Timothy M Albright, Valeria A Moore, Victoria V Bot, Walter L Fava, Wanda Y Fields, Wanda Y Honeyblue, Wayne L Jefferson, William D Bassett, Jr, William D Murray, William F Lagud, Jr, Zachary L Miller

La Tasham Gunter's Documents

Publish Date Document Type Title
November, 2023 FDA 483 Washington Fertility Center - Form 483, 2023-11-02
August, 2017 FDA 483 Grifols Biomat USA Inc. - Form 483, 2017-08-31
November, 2019 FDA 483 Blood Bank of Delmarva, A Division of New York Blood Center, Inc. - Form 483, 2019-11-12
March, 2018 EIR Department of Veterans Affairs Medical Center - EIR, 2018-03-05
August, 2023 FDA 483 Fairfax Cryobank, Inc. - Form 483, 2023-08-24
September, 2019 FDA 483 Octapharma Plasma, Inc. - Form 483, 2019-09-23
February, 2012 FDA 483 Response Inova Health Care Services - Form 483R, 2012-03-15
February, 2012 FDA 483 Inova Health Care Services - Form 483, 2012-03-14
November, 2018 EIR B Positive National Blood Services College Park, LLC - EIR, 2018-11-09
May, 2016 EIR Fisher Bioservices - EIR, 2016-05-20
January, 2023 FDA 483 Dominion Fertility & Endocrinology - Form 483, 2023-01-24
June, 2023 FDA 483 CorneaGen - Boston - Form 483, 2023-06-09
March, 2018 FDA 483 Department of Veterans Affairs Medical Center - Form 483, 2018-03-05
October, 2019 FDA 483 Shady Grove Fertility - Form 483, 2019-10-11
February, 2022 FDA 483 CCRM Fertility Northern Virginia - Form 483, 2022-02-11
March, 2011 FDA 483 Faraway Farms, Inc. - Form 483, 2011-03-30
March, 2020 FDA 483 Shady Grove Fertility - Form 483, 2020-03-02
August, 2019 FDA 483 Pentagon Blood Collection Site - Form 483, 2019-08-22
August, 2019 FDA 483 Inova Health Care Services - Form 483, 2019-08-07
January, 2020 FDA 483 Montgomery Fertility Center - Form 483, 2020-01-21
March, 2012 EIR American Red Cross Blood Services - EIR, 2012-03-19
August, 2017 EIR Grifols Biomat USA Inc. - EIR, 2017-08-31
April, 2024 FDA 483 Supreme Orthopedic Systems - NOVA - Form 483, 2024-04-10
June, 2022 FDA 483 The A.R.T. Institute of Washington, Inc. - Form 483, 2022-06-08
November, 2021 FDA 483 The George Washington University Medical Faculty Associates Fertility and IVF Center - Form 483, 2021-12-13
October, 2024 FDA 483 Department of Defense - Navy - Form 483, 2024-10-03
September, 2024 FDA 483 Inova Health Care Services - Form 483, 2024-09-04
September, 2024 FDA 483 University Of Virginia Health System - Form 483, 2024-09-12
September, 2023 FDA 483 Virginia Center for Reproductive Medicine - Form 483, 2023-09-20

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