FDA Investigator Rendall E Barfoot
Rendall E Barfoot has inspections in 2 countries as of 21 Sep 2023. Rendall E Barfoot has collaborated with a combinined 3054 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
165
Last Inspection Date:
21 Sep 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America
Co-Investigator(s):
Adam C Hipko,
Adrian Rodriguez,
Akbar J Zaidi,
Alan M Roberts,
Alcee M Tavarez,
Andrea J Schmidt,
Andrew A Hoopes,
Andrew K Schaal,
Andrew M Kolenc,
Anh M Lac,
Anna L Tucker,
April K Hill,
Aqualia L Nelson,
Arie R Dyk,
Ashlee M Ward,
Ashley N Williams,
Axel M Ambert,
Azotearc,
Bearde,
Bei Y He,
Betty K Baxter,
Brackens Harris,
Brenda C Hamilton,
Brian R Cronenwett,
Brittany D Terhar,
Bruce E Taylor,
Casey L Hamblin,
Cathleen A Castellaw,
Chad J Whitwell,
Chad W Rice,
Charles D Brown,
Chmura,
Connie L Hannon Rabel,
Danny D Horner,
Darla J Christopher,
Darrah,
David A Gonzalez,
David M Beltran,
Debra L Curtis,
Decarlos A Gomez,
Deniza Karacic,
Dennis R Hudson,
Diana M Guidry,
Edmiston,
Edward D Edmiston,
Elisa M Fleming,
Elizabeth D Connell,
Elkins,
Elvia J Cervantes,
Eric C Nielsen,
Eric M Padgett,
Felix J Marrero,
Frank L Cordova,
Frans E Mercado,
Frederic W French, III,
Glasgow,
Grant,
Grant L Davis,
Gregory A Holt,
Hanna L Potter,
Heath W Cartwright,
Hung V Le,
Isaiah D Isakson,
James J Houlihan,
Jane M Broussard,
Janet B Abt,
Janice M Hickok,
Jeffery A Hangartner,
Jeffrey B Moody,
Jeffrey R Wooley,
Jennifer D Young,
Jennifer Owens Dowdy,
Jennifer R Mathern,
Jodi M Gatica,
Johnson,
Johnsont,
Jonathan A Womack,
Jonathan M Mcbride,
Joseph R Lambert,
Joy L Ramsey,
Juan D Lopez,
Kamara Mo,
Kara L Roden,
Karen C Daugherty,
Karen M Montgomery (KMM),
Kari M Johansen,
Karlton T Watson,
Katherine M Taylor,
Kathleen Chmura Shaffer,
Kayla R Deatherage,
Keith A Harvey,
Keith C Littrell,
Kenitra D Hewitt,
Kevin A Beavers,
Kimberlee A Ewing,
Kristi Mhampton Thurston,
Larisa E Pavlick,
Latorie S Jones,
Lawrence C Coleman,
LCDR Audra J Lenhart,
Linda K Cline,
Linhart,
Lisa D Ellis,
Lisa L Flores,
Lisa M Puttonen,
Lloyd D Payne,
Lourdes R Genera,
Lyndsey G Smith,
Marc A Jackson, Jr,
Marc R Dickens,
Marcia G Evans,
Margaret M Annes,
Martinez,
Mathur,
Matthew B Casale,
Matthew M Schuckmann,
Matthew S Mccollough,
Melinda L Rice,
Merelynn Rhoten,
Michael A Feingold,
Michael S Kopf,
Michelle C Webb,
Michelle D Motsinger,
Monica M Mcclure,
Nancy G Schmidt,
Nancy P Hamburg,
Naseem S Jouhari,
Nathan M Jornod,
Nathan R Moon,
Patricia A Maestas,
Paul E Frazier,
Paula J Perry,
Pauline N Logan,
Payne,
Peter M Boyt,
Pitman,
Quynh Anh H Tran,
Randy V Bong,
Rashonda N Rucker,
Rebecca C O Bryan,
Rhonda L Dash,
Richard D Coleman,
Robert J Ham,
Robert T Harris,
Robert T Lorenz,
Ronda Loyd Jones,
Ronda R Loyd Jones,
Rosanna M Goodrich,
Samuel A Hamblin,
Samuel K Gibbons, Jr,
Samuel R Carter,
Sandy J Ziegler,
Scott R Nichols, PhD,
Scott T Ballard,
Sean M Cheney,
Shanna R Haden,
Shawn E Larson,
Shererk,
Sherrie L Krolczyk,
Staci G Mcallister,
State Agency,
Stephen L Beekman,
Steven A Gonzales,
Steven D Kehoe,
Steven P Allen,
Stroman,
Tamera H Hunt,
Tara A Gray,
Tara M Aikens,
Tara M Humfeld,
Ted L Anderson,
Thuy T Nguyen, LCDR,
Timothy B Webb,
Toby Vern H Hill,
Torrance J Slayton,
Travis D Brown,
Travis S Brown,
Trevor A Parker,
Tricia S Martinez,
Trina K Vick,
Vanessa J Stefka,
Walsworth,
Yaw O Osei,
Zachary L Miller,
Zachary L Stamm
Rendall E Barfoot's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2021 | FDA 483 | Ridley USA Inc. - Form 483, 2021-03-26 |
February, 2021 | FDA 483 Response | Midwestern Pet Foods Chickasha Operation - Form 483R, 2021-02-05 |
August, 2019 | FDA 483 | Texas Tripe - Form 483, 2019-08-26 |
February, 2021 | FDA 483 | Midwestern Pet Foods Chickasha Operation - Form 483, 2021-02-05 |
January, 2017 | FDA 483 | MBDR Foods, LLC - Form 483, 2017-01-17 |
June, 2023 | FDA 483 | Casey Boling - Form 483, 2023-06-22 |
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.
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