FDA Investigator Melissa J Holz

Melissa J Holz has conducted inspections on 111 sites in 3 countries as of 28 Jun 2021. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
111
Last Inspection Date:
28 Jun 2021
Investigator Role:
FDA Investigator
Redica ID:
100000781
Countries of Inspections:
United States of America, Germany, Italy
FDA Investigators that have inspected at least one site in common with Melissa J Holz:
Aaron L Dunbar, Adaliz Santaliz Cruz, Adam J Taylor, Albert L Nguyen, Alecia L Marson, Althea A Williams, Amanda Dinaro, Amir Alavi, Amy L Mcintyre, Anthony L Nicoli, Benjamin W Anderson, Billi Jom Johnson, Boun M Xiong, Burnell M Henry, Catherine M Vanderhoef, Charles R Cote, RIC, Chava Kimchi Sarfaty, PhD, Christina A Castineyra, Christina L Bigham, Christopher D Leach, Cindy Gunnarson, Clifford F Long, Clifton L Randell, Conor J Mccarron, Constance L Richard, Corey K Reno, Courtney R Tiegs, Dale A Nyberg, Darlene L Krieger, Demetria L Lueneburg, Denise L Burosh, Diane T Reindl, Edward E Lockwood (EEL), Elias H Wachter, Eliezar Ramos, Elizabeth B Griffin, Elizabeth E Hart (ASCP), MT, Ellen C Weisensel, Emily S Mcgann, Emma R Schaefer, Emmanuel A Dimaano, Jr, Eric A Breselow, Eric C Fox, Eric T Huebler, George T Allen, Jr, Gloria A Milster, Howard A Burmester, Humera T Khan, Jaclyn N Munsch, Jacqueline Mdiaz Albertini, James A Beaulieu, James M Odonnell, Jamie R Thompson, Jane E Nelson, Janis R Armedoriz, Jean M Bosenbecker, Jeanne M Morris, Jeffry A Bernhardt, Jennifer Guttuso, Jennifer S Ness, Jesse A Vazquez, Jesse P Romenesko, Jessica L Barr, Jessica L Johnson, Jocelyn M Muggli, Joel D Hustedt, John A Iwen, John P Hermann, Joseph M Edwin, Justin A Boyd, Karen M Labounty, Kathryn M Mogen, Keith C Rindahl, Kellie L Thommes, RN, Kellie L Westerbuhr, Kenneth A Libertoski, Kimberly Lewandowski Walker, Kimberly W Destromp, Kip J Hanks, Kirsten L Vadheim, PhD, Lauren M Lilly, PhD, LCDR Debra Emerson, LCDR Ismael Olvera, IV, Lee Terry Moore, Leo J Lagrotte, Lewis K Antwi, Linda V Weyer, Lisa M Lopez, Lisa T Michel, Madeline T Campbell, Marc A Jackson, Jr, Marissa S Steinhagen, Maryann Ruff, Melanie C Voges, Melissa D Kalik, Melissa I Michurski, Melissa J Ireland, Michael A Blaine, Michele L Forster, PhD, Michelle J Glembin, Mihaly S Ligmond, Nicholas T Domer, Nicholas Z Lu, Nicole C Shokatz, Omotunde O Osunsanmi, Paula A Trost, Peter Kessler, PhD, Prabhu P Raju, Rafael A Kaup, Ralph Jerndal, Rebecca L Mullikin, Richard Jay Tucker, RS, Richard M Willey, Richard W Koller, Robert M Tillman, Ronald R Ruff, Sandra A Hughes, Sandra Sejdinovic, Sarah A Palmer, Scott L Schenian, Shafiq S Ahadi, Shalonda C Clifford, Shaquenta Y Perkins, Stephen D Eich, Susan M Matthias, Susan M Miller, Susan M North, Suzanne M Crotty, Tara C Singh, Tara M Carolfi, Tara M Humfeld, Thomas W Garvin, Traci C Kelm, Travis S Bradley, Tyler R Courtney, William F Lagud, Jr, William P Fournier, Yehualashet A Gessesse, Ze Peng, Zoey A Trombley

Melissa J Holz's Documents

Publish Date Document Type Title
March, 2010 FDA 483 Lechnologies Research, Inc. - Form 483, 2010-03-24
January, 2010 FDA 483 GenTrac Inc. - Form 483, 2010-01-28
July, 2010 FDA 483 Cerv-i-trac / Kenneth Yorgan, Dc - Form 483, 2010-07-26
November, 2010 FDA 483 Kerr Corporation - Form 483, 2010-11-16
June, 2009 FDA 483 Preservation Solutions, Inc. - Form 483, 2009-06-12
October, 2012 FDA 483 GE Medical Systems Information Technologies, Inc. - Form 483, 2012-10-09
January, 2012 FDA 483 Froedtert Hospital Reproductive Medicine Center - Form 483, 2012-01-11
October, 2009 FDA 483 CRS Medical Diagnostics, Inc - Form 483, 2009-10-01
April, 2012 FDA 483 Converting Biophile Laboratories, Inc. - Form 483, 2012-04-03
November, 2012 FDA 483 Perfecseal, Inc. - Form 483, 2012-11-30
November, 2012 EIR Perfecseal, Inc. - EIR, 2012-11-30
January, 2013 FDA 483 Frontier Medical Products Inc. - Form 483, 2013-01-10
January, 2011 FDA 483 Datex-Ohmeda, Inc. - Form 483, 2011-01-28
October, 2011 FDA 483 Wisconsin Pharmacal Company, LLC - Form 483, 2011-10-12
January, 2010 EIR GenTrac Inc. - EIR, 2010-01-28
October, 2010 FDA 483 TreyMed, Inc. - Form 483, 2010-10-06
January, 2013 FDA 483 Electro Kinetic Technologies, LLC - Form 483, 2013-01-17
October, 2012 FDA 483 Young Microbrush, LLC dba Microbrush International - Form 483, 2012-10-22
June, 2012 FDA 483 GF Health Products, Inc./d.b.a.Basic American Metal Products - Form 483, 2012-06-12
March, 2010 FDA 483 Arch - MedTorque Inc. - Form 483, 2010-03-18
March, 2013 FDA 483 Prism Clinical Imaging Inc. - Form 483, 2013-03-06
May, 2010 FDA 483 Performance Health Supply Inc. - Form 483, 2010-05-21
September, 2011 FDA 483 GF Health Products, Inc./d.b.a.Basic American Metal Products - Form 483, 2011-09-23
March, 2012 FDA 483 GE Medical Systems, LLC - Form 483, 2012-02-27
March, 2010 FDA 483 OCENCO, INCORPORATED - Form 483, 2010-03-11
March, 2013 FDA 483 Imaging Biometrics LLC - Form 483, 2013-03-22
July, 2013 FDA 483 InControl Medical, LLC - Form 483, 2013-07-17
October, 2014 FDA 483 TreyMed, Inc. - Form 483, 2014-10-21
July, 2012 FDA 483 Norland, A CooperSurgical Company - Form 483, 2012-07-30
January, 2012 FDA 483 Reproductive Specialty Center Ltd - Form 483, 2012-01-25
April, 2012 FDA 483 OCENCO, INCORPORATED - Form 483, 2012-04-20
July, 2012 FDA 483 Wisconsin Pharmacal Company, LLC - Form 483, 2012-07-11

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