FDA Investigator David M Wilkinson

David M Wilkinson has inspections in 3 countries as of 17 Oct 2023. David M Wilkinson has collaborated with a combinined 985 experts on various inspections, contributing to compliance and improvement across diverse sectors.

Investigator Details

Number of Inspected Sites:
45
Last Inspection Date:
17 Oct 2023
Investigator Role:
FDA Investigator
Redica ID:
100004900
Country:
Denmark, United States of America, Germany
Co-Investigator(s):
Abraham M Maekele, Alex J Wild, Althea A Williams, Angela E Glenn, Arduino Frankovic, Ashley A Mutawakkil, Ashley A Segura, Brandon P Thompson, CDR Ileana Barreto Pettit, CDR Sean T Creighton, Charlotte P Chang, Clifford F Long, Dawn M Mccabe, Dianiris C Ayala, Dionne D Arline, Donald J Mee, Dorothy W Lee, Ebony D Sanon, Edwards, Edwin J Gorney, Eric R Holm, Gabriel E Muniz, Gisselle I Sensebe, Harry R Bringger, Jr, Hunt, Iris C Macinnes, Ivan E Reyes, Jennifer L Huntington, Jontae D Sanders, Joshua J Silvestri, Karen M Rodriguez, Karl D Hezel, Kelly I Anderson, LCDR Angelica M Chica, Leo J Lagrotte, Lisa A Warner, Marc Balzarini, Mark E Chan, Mark F Chan, Mendoza, Michael D Gifford, Michelle S Dunaway, Monica Cburgos Garcia, Omayra Nrodriguez Ruiz, Patricia A Mcilroy, Paul A Licata, Richard K Vogel, Salvatore N Randazzo, Sara M Onyango, Saundrea A Munroe, Sergio E Delgado, Stanley B Eugene, BS, BME, State Agency, Stephanie D Crockett, Suzanne A Lovelady, Thomas J Hudson

David M Wilkinson's Documents

Publish Date Document Type Title
April, 2018 FDA 483 International Medical Industries, Inc. - Form 483, 2018-04-03
October, 2019 FDA 483 Carroll-Baccari, Inc. - Form 483, 2019-10-16
April, 2018 EIR International Medical Industries, Inc. - EIR, 2018-04-03
April, 2022 FDA 483 Powers Medical Devices, LLC - Form 483, 2022-04-29
December, 2019 FDA 483 FloSpine, LLC - Form 483, 2019-12-13
February, 2023 FDA 483 Stingray Surgical Products, LLC - Form 483, 2023-02-09
August, 2022 FDA 483 Medscience Research Group Inc - Form 483, 2022-08-26
February, 2019 FDA 483 Curonix LLC - Form 483, 2019-02-15
December, 2018 FDA 483 Protech Leaded Eyewear - Form 483, 2018-12-14
September, 2021 FDA 483 Technological Medical Advancements LLC - Form 483, 2021-09-09
March, 2019 FDA 483 Bonafix Surgical and Dental Implants, LLC - Form 483, 2019-03-11
December, 2017 FDA 483 Fen Dental Manufacturing, Inc. - Form 483, 2017-12-01
December, 2017 FDA 483 Modal Manufacturing, LLC - Form 483, 2017-12-08
April, 2019 FDA 483 SurGenTec, LLC - Form 483, 2019-04-18
November, 2019 FDA 483 Ceragroup Industries Inc - Form 483, 2019-11-25
October, 2021 FDA 483 EUSA Global, LLC - Form 483, 2021-10-15
May, 2018 FDA 483 HNM Total Recon, LLC - Form 483, 2018-05-09
May, 2022 FDA 483 ULTRAVISION CORPORATION - Form 483, 2022-05-20
May, 2023 FDA 483 Faico Medical LLC - Form 483, 2023-05-02
August, 2019 FDA 483 3D Medical Manufacturing, Inc. - Form 483, 2019-08-23
February, 2020 FDA 483 Technological Medical Advancements LLC - Form 483, 2020-02-24
March, 2022 FDA 483 Craftmatic Industries, Inc. - Form 483, 2022-03-07
February, 2018 FDA 483 Mako Surgical Corporation - Form 483, 2018-02-23
October, 2023 FDA 483 Bing Innovations Llc - Form 483, 2023-10-17
July, 2023 FDA 483 Fettech - Form 483, 2023-07-14
November, 2023 FDA 483 Oxygen Therapy Institute - Form 483, 2023-11-17

Experience Redica System's 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