FDA Investigator Travers

Travers has inspections in 1 countries as of 14 Sep 2023. Travers has collaborated with a combinined 2119 experts on various inspections, contributing to compliance and improvement across diverse sectors.

Investigator Details

Number of Inspected Sites:
233
Last Inspection Date:
14 Sep 2023
Investigator Role:
FDA Investigator (Contractor)
Redica ID:
Country:
United States of America
Co-Investigator(s):
Abdellah El Hajjam, Alan D Centi, Alfred Puglia, Anastasia M Shields, Anita R Michael, Ann Marie Karnick, Anna Lazar, Anne E Johnson, Audrey Thereset Uy, Brandi L Garbutt, Brandon J Brookens, Brandon M Kurjanowicz, Brian D Young, Brian S Keefer, Calvin W Edwards, Cara M Minelli, Carl E Lovrich, CDR Michael J Mero, Chamberlain, Charlotte E Wilkins, Crayton Lee, Crystal A Harlan, Cynthia L Rakestraw, Cynthia White, Daniel T Lee, Daniel W Johnson, Darlene C Plank Turlington, Dauksism, David A Schwartz, Derek S Dealy, Dessa A Antoine, Donyel M Jones, Dougherty, Doyle, Dr. Mark J Seaton, PhD, Edward D Mcdonald, Edwin L Hobbs, Eric S Myskowski, Erica L Nicoll, Erika M Wilkerson, Gayle S Lawson, Gerald W Kopp, Gess, Gladys B Casper, Greg Phillips, Gregory E Beichner, Hala L Selby, James M Mason, James M Odonnell, James P Mcevoy, Jane M Broussard, Jeannie R Mayberry, Jeen S Min, Johnsona, Joseph Brady, Joseph L Despins, PhD, Joseph R Hatcher, Joseph S Fanelli, Joseph T Dougherty, Joshua C Schafer, Judith A Paterson, Julianne C Mccullough, Kailee R Mason, Katelyn Astaub Zamperini, Kendra L Brooks, Kim G Campbell, Kirk A Dymbrowski, Kristina J Donohue, Kyle D Covill, Kyle S Hobson, LCDR Margaret E Digennaro, LCDR Susan E Polifko, LCDR William H Bender, Linda M Hoover, Linda M Ross, LT John M Mastalski, LTJG Bradley E Benasutti, LTJG Lauren N Shade, Magda M Karlsen, Magdi A Ali, Marc A Jackson, Jr, Marjorie L Davis, Martha Sullivan Myrick, Mary R Kirker, Matthew R Noonan, Maureen A Wentzel, Meredith L Sheridan, Michael A Taylor, Michael J Diskin, Michael J Nerz, Michael Rosner, Mike M Rashti, Myrick, Nancy M Lazzari, Nikisha M Bolden, Osama M Hamoud, Princess R Campbell, Raffi B Papazian, Robert B Shibuya, MD, Ronald T Colucci, Russell P Vandermark, Ruth A Oni, Sarah K Lemin, Sean D Duke, Seng Ching Hwang, Sharon Mills, State Agency, Stephanie Mangigian, MS/OSH, RN, Steven E Kane, Sullivanm, Tammy M Phillips, Thomas E Friel, Timothy J Schmidt, Todd J Maushart, Tonya O Corbin, Travis R Hunt, Valeria A Moore, Vlada Matusovsky, Whitney S Reynolds, William C Brenneman, Xinyi Hui, Yessika Mashinski

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