FDA Investigator Martin J Guardia

Martin J Guardia has inspections in 1 countries as of 23 Aug 2023. Martin J Guardia has collaborated with a combinined 3239 experts on various inspections, contributing to compliance and improvement across diverse sectors.

Investigator Details

Number of Inspected Sites:
151
Last Inspection Date:
23 Aug 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America
Co-Investigator(s):
Abby E Pelletier, Alan R Condon, Alice C Silva, Alois P Provost, Alysia M Salonia, Alyssa R Favro, Amber G Wardwell, Amy C Jordan, Andrew J Seaborn, Andrew M Barlow, Andrew P Abban, Ann L Simoneau, Anne E Carpenter, Anthony C Warchut, Anthony N Onianwa, Anthony P Costello, Anthony W Thomas, Arie C Menachem, Ashley M Whitehurst, Atricia L Irons, Bradford L Swanson, Bradley D Newsad, Brandy L Couillard, Brandy L Gillilan, Brenda P King, Brenna L Macdowell, Bruce R Ota, Carl A Huffman, III, Carla C Tuite, Charles A Snipes, PhD, Charles R Bonapace, PhD, Christine L Williams, Christopher A Demitrius, Christopher K Vantwuyver, Christopher M Elliott, Constance Desimone, Courtney N Long, Cynthia A Harris, MD, RN, Daniel E Needham, Darin S Wiegers, David P Vanhouten, David S Firley, Dawn M Braswell, Dean R Rugnetta, Debra D Devlieger, Diantha M Turner, Dorothy W Lee, Douglas Florentino, Douglas S Joslin, Dr. Abhijit Raha, PhD, Dr. Mark J Seaton, PhD, Dr. Sriram Subramaniam, PhD, Dr. Zhou Chen (nmi), MD PhD, Edmund F Mrak, Jr, Eduardo L Rodriguez, Elizabeth B Griffin, Ellen P Madigan, Emily J Schramm, Erich P Garger, Erik W Koester, Erin P Conlin, Frank J Koch, Frank K Fulford, Gam S Zamil, Garry H Stewart, Gary J Hagan, Gary S Hagan, George T Allen, Jr, Gerard D Difiore, Greg W Hites, Intkhab H Wahla, Irons, Isaac K Carney, James W Whitney, Jamie S Mathews, Jason A Rossi, Jason D Tenney, Jay M Patria, Jayaleka J Amarasinghe, Jeffrey S Buckser, Jessica D Spellman, Jessica I Newman, John J Thibodeau, John L Zaccone, John P Shelton, John R Carlson, John S Hartford, Jonathan B Lewis, Joppie, Jose A Torres, Joseph B Cascio, Joseph Foley, Joseph H Procopio, Joseph T Frost, Joyce A Kellett, Joyce A Williams, Justine M Corson, Karen Mcnabb Noon, Kathleen A Sousa, Kathleen E Mcafoose, Kathleen M Curry, Kenneth H Williams, Kent A Conforti, Kimberly J Langello, Kristina J Donohue, Lauren M Lawrance, Laurie B Frazier, LCDR Debra Emerson, Leo B Zadecky, Liz M Otero, Lorayne A Mcguinness, Lori S Lawless, Louis Christy, M Patriciaurphy Murphy, Marc S Neubauer, Mark E Farrell, Mark K Tseng, Mark R Mcclain, Mary Jeanet Mcgarry, Matthew C Watson, Maxim, Maya M Davis, Mclaughlin, Megan A Haggerty, Michael E Antaya, Michael F Skelly, PhD, Michael P Sweeney, Michelle M Noe, Michelle M Noe Varga, Mikayla K Deardorff, Nabil Nakhoul, Nasser Yazdani, Nichole B Murphy, Osama A Khatib, Pamela L Ogonowski, Paraluman S Leonin, Patrick M Regan, Paul P Geraci, Paula M Laplant, Philip Kreiter, Ramcharan S Khalsa, Ramon E Martinez, Rebecca A Coleman, Remal, Richard F Hapke, Richard H Penta, Richard L Licari, Robert D Ogan, Robert E Teel, Robert J Martin, Robert Mo Brien, Rory K Geyer, Rupa Pradhan, Sandra P White, Sean M Tessicini, Sean R Marcsisin, Sharon Rhew, Slater K Bartlett, State Agency, Stephanie M Roberts Pedotti, Stephen C King, Stephen C Smith, Stephen R Souza, Steven M Ferrara, Susanne M Richardson, MSc RAC ELS, Sylvia A Craven, Tania K Mercado, Teddy Tom, Thomas Cote, Thomas H Jenkins, Thomas J Murphy, Thomas O Morgan, Thomas Siebertz, Thomas W Nerney, Timothy M Glod, Troy R Petrillo, Victor J Gangi, Victoria M Daddeo, Victoria Taylor, Wendy A Johnecheck, Weston K Szymanski, William K Dagley, Willis I Cobb Jr

Martin J Guardia's Documents

Publish Date Document Type Title
December, 2007 FDA 483 Response Labcorp Bedford LLC. - Form 483R, 2007-12-13
December, 2007 FDA 483 Labcorp Bedford LLC. - Form 483, 2007-12-07
September, 2003 FDA 483 Charles River Laboratories Preclinical Services - Form 483, 2003-09-25
December, 2007 EIR Labcorp Bedford LLC. - EIR, 2007-12-07
September, 2003 EIR Charles River Laboratories Preclinical Services - EIR, 2003-09-23

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