FDA Investigator Bruce E Kummer
Bruce E Kummer has conducted inspections on 303 sites in 1 countries as of 17 May 2012. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
303
Last Inspection Date:
17 May 2012
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Bruce E Kummer:
Alan Escalona,
Amos C Epps,
Amy C Amaro,
Ana P Barido,
Andrew M Kupper,
Andrew T Todd,
Austin B Appler,
Barbara A Gullick,
Brandon L Mariner,
Brian M Palermo,
Brian R Yaun,
Bruce C Kovak,
Carol A Robles,
Carrie L Doupnik,
Chaltu Nwakijra,
Charlotte E Wilkins,
Christopher L Taste,
Christopher R Richardson,
David G Whitman,
David P Rice, Jr,
Dawn M Collins,
Decima L Washington,
Dennis L Doupnik,
Deyaa Shaheen,
Edward P Potter,
Elvis D Morton,
Emmanuel A Dimaano, Jr,
Geoffrey M Leist,
Heath R Harley,
Jacqueline Johnson,
Jamie D Richardson,
Jamie D Swann,
Jessica D Nanini,
Jessica D Weber,
Joey C West,
John Dan,
John M Gusto,
Johnson,
Jonathan W Chapman,
Julie A Silberberg,
Justin C Fuller,
Kasey J Hollobaugh,
Katherine E Jacobitz,
Kenneth L Smalls,
Kenya K Moon,
Lara M Snyder,
Laurissa S Flowers,
Lawrence C Edwards,
LCDR Cornelius Brown, III,
LCDR Matthew R Mcnew, MPH, REHS/RS,
LCDR Wilfred A Darang,
Marcus A Ray,
Margaret H Waters,
Margo C Jones,
Marla A Cassidy,
Michael D Garcia,
Michael S Call,
Michele R Douglas,
Michelle E Noonan Smith,
Mohamad A Chahine,
Nancy L Meade,
Natasha A Dezinna,
Nianna C Burns,
Osama M Hamoud,
Philip W Beck,
Renisha M Shaw,
Richard G Runyon,
Rina Bhikha,
Russell R La Claire,
Sara Jdent Acosta,
Sean R Moynihan, MPH,
Shelby W Brown, Jr,
Sierra M Shockley,
Stephen C Eason,
Steven P Donald,
Tajah L Blackburn,
Tamara N Champion,
Tania E Vizcaino,
Terrance L Thomas,
Thomas C Woods,
Thomas J Hudson,
Thomas R Withers,
Tiki J Dixon,
Timothy M Albright,
Valeria A Moore,
Wayne L Jefferson,
William A Warnick,
William D Bassett, Jr,
William D Murray,
Yvonne T Lacour,
Zhongren Wu
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](/images/InspectorProfile.png)
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