FDA Investigator Jennifer S Ness

Jennifer S Ness has conducted inspections on 164 sites in 11 countries as of 08 Jun 2022. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
164
Last Inspection Date:
08 Jun 2022
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America, France, Netherlands, Germany, Italy, Canada, Slovakia, China, Australia, Finland, United Kingdom of Great Britain and Northern Ireland
FDA Investigators that have inspected at least one site in common with Jennifer S Ness:
Aaron L Dunbar, Aimee J Edwin, Alan R Albrecht, Albert L Nguyen, Alexandria L Capuano, Alison A Nicoli, Althea A Williams, Amanda Dinaro, Amy L Mcintyre, Andrew A Hoopes, Anthony J Ladner, April L Brown, April L Young, Arthur G Hurst, Aswin T Subketkaew, Barbara Janine Breithaupt, Benjamin W Anderson, Billi Jom Johnson, Boun M Xiong, Bradley A Servais, Brandi L Garbutt, Brent T Hall, Brittany D Terhar, Candace S Tucker, Carolyn A Warren, Catherine J Laufmann, Charles R Cote, RIC, Christina L Bigham, Christine I Shaw, Clifford F Long, Corey K Reno, Coreyk Zelinski, Courtney R Tiegs, Dacia E Quick, Dale A Nyberg, Daniel J Lahar, David P Rice, Jr, Deborah A Greco, Demetria L Lueneburg, Denise L Burosh, Denise R Beuttenmuller, Dianiris C Ayala, Dolores Harper, Donna Ltartaglino Besone, Douglas W Atkins, Duc Minh H Nguyen, Edward E Lockwood (EEL), Emma R Schaefer, Eric C Fox, Eric M Padgett, Eric T Huebler, Esteban Beltran, Evelyn Taha, Fannie M Harrell, Francis A Guidry, Gregory A Berg, Gregory W Smith, Gregson A Joseph, Heidi J Debeck, Ivan E Reyes, Jaclyn N Munsch, Jacqueline S Warner, James A Beaulieu, James D Planchon, James K Ireland, James P Mcreavey, Jamie P Webb, Janis R Armedoriz, Jennifer A Robinson, Jessica L Johnson, Jocelyn M Muggli, Joey C West, John A Sciacchitano, John E Emmert, Joseph A Piechocki, Joseph D Gong, Joseph M Edwin, Joshua J Silvestri, Justin A Boyd, Justin A Hefferman, Justin J Jafferis, Karen M Labounty, Karla J Youngberg, Kellie L Thommes, RN, Kellie L Westerbuhr, Kelvin Cheung, Kenneth A Libertoski, Kevin P Regan, Kimberly Lewandowski Walker, Kimberly M Lichter, Kirtida Patel, Kyle J Mccracken, Ladislav Kermet, Laiza V Garcia, Lauren E Priest, LCDR Wilfred A Darang, Linda V Weyer, Lisa M Lopez, Lori A Carr, Lori S Lawless, Luz I Collado, Mada A Tautges, Maria E Treadwell, Maribeth G Niesen, Marie A Fadden, Marissa S Henning, Marissa S Steinhagen, Martina E Lagrange, Mary A Millner, Mary K Concannon, Melanie G Warzala, Melanie W Pishnery, Melinda B Lewis, Melissa D Kalik, Melissa I Michurski, Melissa J Holz, Michael J Nerz, Michelle J Glembin, Mildred J Tures, Msdap Gonzlezk, Nicholas T Domer, Nicholas Z Lu, Nicole C Victoria, PhD, Paola E Lathrop, Perry H Gambrell, Rafael A Kaup, Rafael Padilla, Ralph Jerndal, Rhonda L Mecl, Richard Jay Tucker, RS, Robert G Antonsen, Jr, Rosanna M Goodrich, Ross J Grigsby, Ryan J Benedict, Sandra A Hughes, Sarah A Palmer, Scott A Golladay, Scott B Laufenberg, Seth A Abbott, Sharon I Gundersen, Sharon K Thoma, PharmD, Sharon L Matson, Shawn Choi, Sherry L Secrist, BLT DO, Sonya L Karsik, RAC, Stephen D Eich, Susan M Atcher, Susan M Matthias, Tara C Singh, Thanh M Andrews, Thomas E Friel, Thomas W Garvin, Tiffany P Kelley, Timothy G Philips, Timothy R Marrs, Tony T Yang, Tyler R Courtney, Wendy L Trefethren Grang, William D Bassett, Jr, Yehualashet A Gessesse

Jennifer S Ness's Documents

Publish Date Document Type Title
February, 2021 FDA 483 Cirtec Medical Corporation - Form 483, 2021-02-25
September, 2018 FDA 483 Medspira, Llc - Form 483, 2018-09-06
October, 2014 FDA 483 Blue Belt Technologies inc - Form 483, 2014-10-01
August, 2017 FDA 483 MR Instruments Inc - Form 483, 2017-08-02
October, 2019 FDA 483 Deerfield Imaging, Inc. - Form 483, 2019-10-01
October, 2021 FDA 483 Beckman Coulter, Inc. - Form 483, 2021-10-28
December, 2018 FDA 483 Exercore, LLC - Form 483, 2018-12-18
August, 2018 FDA 483 Clarus Medical, Llc - Form 483, 2018-08-23
June, 2015 FDA 483 Datex-Ohmeda, Inc. - Form 483, 2015-06-12
April, 2022 FDA 483 Revolutionary Science - Form 483, 2022-04-06
January, 2020 EIR Vesta Inc. - EIR, 2020-01-31
July, 2018 FDA 483 Celfa s.c. - Form 483, 2018-07-20
July, 2018 FDA 483 Cefla s.c - Form 483, 2018-07-20
February, 2020 FDA 483 Creganna Medical - Form 483, 2020-02-28
August, 2017 EIR SAFC Inc - EIR, 2017-08-23
December, 2021 FDA 483 Response Microbiologics Inc - Form 483R, 2021-12-22
December, 2021 FDA 483 Microbiologics Inc - Form 483, 2021-12-01
July, 2021 FDA 483 Katecho LLC - Form 483, 2021-07-16
August, 2021 FDA 483 RxFunction Inc. - Form 483, 2021-08-06
August, 2017 FDA 483 Birchwood Laboratories LLC - Form 483, 2017-08-18
October, 2014 FDA 483 Respiratory Technologies, Inc. - Form 483, 2014-10-09
February, 2021 EIR St. Jude Medical - EIR, 2021-02-08
June, 2018 FDA 483 GE Medical Systems, LLC - Form 483, 2018-06-14
July, 2015 FDA 483 Somnetics International, Inc. - Form 483, 2015-07-28
April, 2019 FDA 483 Caerus Corp. dba Orthocor Medical - Form 483, 2019-04-24
May, 2019 FDA 483 Vasamed, Inc. - Form 483, 2019-05-16
March, 2019 FDA 483 Acist Medical Systems - Form 483, 2019-03-04
July, 2019 FDA 483 Kimberly-Clark Corp. - Form 483, 2019-07-25
December, 2021 FDA 483 Mivi Neuroscience Inc - Form 483, 2021-12-14
April, 2022 FDA 483 rms Surgical - Form 483, 2022-04-01

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