FDA Investigator Travis S Brown
Travis S Brown has conducted inspections on 207 sites in 3 countries as of 08 Mar 2021. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
207
Last Inspection Date:
08 Mar 2021
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America,
Spain,
Vietnam
FDA Investigators that have inspected at least one site in common with Travis S Brown:
Adam C Hipko,
Adrian Rodriguez,
Alanna L Mussawwir Bias,
Alcee M Tavarez,
Alokita N Karmakar,
Amanda J White,
Amy M Oliver,
Andrew B Bevill,
Angela Mock,
Anh M Lac,
Ashley N Williams,
Astrid M Rylander,
Axel M Ambert,
Betsy C Galliher,
Bing Lin,
Bonnie L Menzel,
Brackens Harris,
Brandi E Williams,
Brandon K Barbee,
Brian P Hendrickson,
Brian R Yaun,
Brook Shea,
Camerson E Moore,
Camille D Brown,
Carol A Declouette Wilburn,
Casey L Hamblin,
Cathleen A Castellaw,
Charles B Steinmiller,
Charles D Brown,
Christina E Muhn,
Christine L Williams,
Christopher D Rush,
Christopher J Hurst,
Christopher J Smith,
Christopher K Gibbs,
Clinton K George,
Crystal A Harlan,
Dallas E Gilbreath Jr,
Danielle Lyke,
Danny D Horner,
Darla J Christopher,
David J Leray,
Debbie J Cunningham,
Decarlos A Gomez,
Denise Connelly,
Deniza Karacic,
Dennis R Hudson,
Dirk L Lincoln,
Douglas J Snyder,
Ed Gonzalez Vazquez,
Edmiston,
Edward D Edmiston,
Elisa M Fleming,
Elizabeth D Connell,
Elmina E Akwo,
Elmina E Mboh,
Enspect User,
Ernest Serna, III,
Fernando C Martinez,
Florecia S Philogene,
Franklin R Harris,
Frans E Mercado,
Frederic W French, III,
Gatica,
Gery M Duparc,
Glasgow Glasgow,
Grant L Davis,
Hung V Le,
Iris C Macinnes,
J Elkins,
Jacey Roy,
Jacob W Reynolds,
James H Robinson,
Jamie L Port,
Jamie M Bumpas,
Jane M Broussard,
Janice M Hickok,
Jeffrey C Archer,
Jeffrey R Wooley,
Jennifer D Young,
Jennifer Hua,
Jennifer O Dowdy,
Jodi M Gatica,
Johann M Fitch,
John Diehl,
Johnson,
Jonathan A Womack,
Jonathan M Mcbride,
Joshua L Gibbs,
Joy L Ramsey,
Juan D Lopez,
Kamara Tx,
Karen C Daugherty,
Kari M Johansen,
Kathleen Chmura Shaffer,
Kayla R Deatherage,
Keegan B Mixon,
Keith A Harvey,
Kelly C Ely,
Kenitra D Hewitt,
Khunnathee Stoner,
Kristen E Szenderski,
Kunapuli T Madhusudhan,
L Grant,
Latorie S Jones,
Lauren E Skokan,
Lauren R Brady,
Lauren R Howell,
Leighton Kn Gai,
Lisa M Puttonen,
Lisa R Jennings,
Lloyd D Payne,
Lorie S Hannappel,
Lourdes Andujar,
Lourdes R Genera,
Maira P Brading,
Marc R Dickens,
Margaret M Annes,
Martha S Baldwin,
Martin K Essary,
Matthew H Pitts,
Matthew R Maddox,
Matthew S Mccollough,
Michael L Jones,
Michelle C Webb,
Monique Rac Lester,
Nicole C Mayfield,
Ninfa N Innocent,
Patrice S Hall,
Patty P Kaewussdangkul,
Paul E Frazier,
Paul Klug,
Payne,
Rachel C Dailey,
Rebecca Co Bryan,
Rendall E Barfoot,
Rene R Ramirez,
Rian L Pope,
Richard T Riggie,
Robert T Harris,
Robert T Lorenz,
Rostislav Servetnyk,
Roy Baby,
Samuel A Hamblin,
Samuel R Carter,
Sandy J Ziegler,
Sara A Valenzuela,
Scott R Nichols, PhD,
Scott T Ballard,
Sean M Cheney,
Selina M Mata,
Seri L Essary,
Shawn E Larson,
Staci G Mcallister,
Tamera H Hunt,
Tara A Gray,
Terrance L Thomas,
Thomas J Hudson,
Timothy B Webb,
Toby Vern H Hill,
Tonya R Johnson,
Torrance J Slayton,
Tracy J Washington,
Travis D Brown,
Travis M Beard,
Tricia S Martinez,
Trina K Vick,
William A Warnick,
Yaw O Osei,
Young M Yoon
Travis S Brown's Documents
Publish Date | Document Type | Title |
---|---|---|
April, 2015 | FDA 483 | Blue Bell Creameries, LP - Form 483, 2015-04-23 |
April, 2015 | FDA 483 Response | Blue Bell Creameries, LP - Form 483R, 2015-08-28 |
May, 2016 | FDA 483 | Dairy Farmers of America, Inc. - Form 483, 2016-05-26 |
November, 2018 | FDA 483 | McDaniel Life-Line LLC - Form 483, 2018-11-16 |
November, 2018 | FDA 483 Response | McDaniel Life-Line LLC - Form 483R, 2018-12-03 |
August, 2018 | EIR | FOCUS Laboratories, Inc. - EIR, 2018-08-28 |
August, 2015 | EIR | Brenntag Southwest, Inc - EIR, 2015-08-19 |
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.

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