FDA Investigator Eric C Schmitt

Eric C Schmitt has conducted inspections on 71 sites in 5 countries as of 06 Nov 2023. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
71
Last Inspection Date:
06 Nov 2023
Investigator Role:
FDA Investigator
Redica ID:
100001933
Countries of Inspections:
United States of America, Germany, Switzerland, Italy, Costa Rica
FDA Investigators that have inspected at least one site in common with Eric C Schmitt:
Abby E Pelletier, Alice C Silva, Althea A Williams, Amy M Cramer, Andrew J Garufi, Angel Asoler Garcia, Anthony N Onianwa, Arie C Menachem, Brenda P King, Camerson E Moore, Christopher J Cruciotti, Darin S Wiegers, Daryl A Dewoskin, David P Vanhouten, Dawn M Braswell, Diane C Thibodeau, Diane M Biron, Diantha M Turner, Dien N Nguyen, Dolores Harper, Dominic R Frasca, Edmund F Mrak, Jr, Edward J Janik, Elizabeth B Griffin, Ellen P Madigan, Gale E Ryan, George T Allen, Jr, Helen B Ricalde, James P Finn, James W Whitney, Janete F Guardia, Jason A Rossi, Jeffrey J Thibodeau, John A Sciacchitano, Jonah S Ufferfilge, Jonathan B Lewis, Jonathan G Matrisciano, Justine M Corson, Katarzyna Plona, Kathleen E Mcafoose, Kimberly J Langello, Lauren M Lawrance, Lauren M Mclaughlin, Laurie B Frazier, LCDR Chad N Thompson, Lynne M Dwyer, Marcia M Laughrey, Maricelys Mercado, Mark R Mcclain, Maryam Tabatabaie, Matthew C Watson, Maura Rooney, Maya M Davis, Megan A Haggerty, Meisha A Mandal, Michael G Mayfield, Michael J Leal, Michael P Anthony, Michael P Sweeney, Michelle M Noe Varga, Mutahar S Shamsi, Nealie C Newberger, Nicholas C Mendiola, Pamela N Agaba, Paul M Kawamoto, Paul P Geraci, Philip H Lafleur, Preston M Lee, Rajiv R Srivastava, Rebecca B Welch, Robert J Martin, Sandra P White, Sara M Onyango, Shawn M Bogdan, Sherry M Nisson, Sonya L Karsik, RAC, Stephen C Smith, Suzanne M Healy, Tamara S Rosbury, Tanya R Syffrard, Tina A Desorcy, Tomika L Crafter, Xiaojun Yan, Yuan Fang

Eric C Schmitt's Documents

Publish Date Document Type Title
February, 2023 FDA 483 Pausch Medical GmbH - Form 483, 2023-02-24
December, 2022 FDA 483 American Performance Polymers, LLC - Form 483, 2022-12-21
June, 2016 FDA 483 Carolina Precision Technologies - Form 483, 2016-06-27
October, 2019 FDA 483 Unetixs Vascular, Inc. - Form 483, 2019-10-29
October, 2017 FDA 483 Network Medical Products (USA) Inc. - Form 483, 2017-10-16
June, 2022 FDA 483 Karl Storz Endovision, Inc. - Form 483, 2022-06-14
May, 2019 FDA 483 Carwild Corporation - Form 483, 2019-05-16
October, 2016 FDA 483 High Technology, Inc. - Form 483, 2016-10-18
August, 2022 FDA 483 UFP Technologies, Inc. - Form 483, 2022-08-17
January, 2016 FDA 483 Kinetic Instruments, Inc. - Form 483, 2016-01-06
November, 2021 FDA 483 MIRA, Inc. - Form 483, 2021-11-18
March, 2022 FDA 483 Bio-Med Devices, Inc. - Form 483, 2022-03-31
July, 2016 FDA 483 Maine Oxy-Acetylene Supply Company - Form 483, 2016-07-27
August, 2018 FDA 483 Atrium Medical Corporation - Form 483, 2018-08-02
December, 2016 FDA 483 OBP Medical Corporation - Form 483, 2016-12-09
May, 2023 EIR CooperSurgical, Inc. - EIR, 2023-06-30
May, 2019 EIR Carwild Corporation - EIR, 2019-06-17
October, 2017 FDA 483 On Site Gas Systems Inc. - Form 483, 2017-10-03
April, 2022 FDA 483 Simply Clean Air & Water Inc. - Form 483, 2022-04-29
October, 2022 FDA 483 Ikonisys Inc. - Form 483, 2022-10-12
August, 2023 FDA 483 Asept Pak Inc. - Form 483, 2023-08-04
June, 2016 FDA 483 Carwild Corporation - Form 483, 2016-06-03
March, 2017 FDA 483 Jensen Industries, Inc. - Form 483, 2017-03-21
February, 2024 FDA 483 Professional Contract Sterilization, Inc. - Form 483, 2024-02-16
June, 2024 FDA 483 Integra LifeSciences Corporation - Form 483, 2024-06-05

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