FDA Investigator Tallman
Tallman has inspections in 1 countries as of 23 Oct 2023. Tallman has collaborated with a combined 1551 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
181
Last Inspection Date:
23 Oct 2023
Investigator Role:
FDA Investigator (Contractor)
Redica ID:
Country:
United States of America
Co-Investigator(s):
Aaron P Wozniak,
Abdur Rashid,
Alaric C Denton,
Allen T Proxmire,
Amy H Ruble,
Andrea Lwilliams Jones,
Arthur G Hurst,
Bernadette T Tallman,
Betsy C Galliher,
Billy M Battles,
Brandy D Brown,
Brian R Yaun,
Bridegan,
Brown,
Cheryl D Barton,
Chestnut,
Chris Alexander,
Christine M O'leary,
Christopher C Wilcox,
Constance Y Fears,
Contractor Bridgers,
Cordelia J Brammer,
David P Moorhead,
David T Glover,
David Williams,
Davis,
Debra J Tucker,
Deyaa Shaheen,
Douglas L Page,
Edward Deberry,
Eileen J Bannerman,
Gamal A Norton,
Garcia,
Gary E Coleman, Jr, REHS,
Gates E Raynor,
Gray,
Harmon,
Heather M Wheeler,
Hristu B Chepa,
Igbinoba,
Ivery,
Jacqueline D Mitchell,
James P Lewis, Jr,
Jeff M Uriarte,
Joe A Odom,
John D Lloyd,
John E Aghadia,
Johnson,
Joseph F Owens,
Kara D Miller,
Katelynn J Rollins,
Kewes,
Kimberly Cdelk Brooks,
Kunapuli T Madhusudhan,
Lakisha N Morton,
Laura D Cain,
Lauryl A Smith,
Lawrence,
Mancia R Walker,
Marcella D Crook,
Marie F Morin,
Marla A Cassidy,
Marybeth Willis,
Matthew G Brown,
Metitia G Sanders,
Metitia M Gramby,
Michael M Quinn,
Michelle D Haamid,
Michelle L Jones,
Nancy E Fontaine,
Nicole D Lyons,
Perry H Gambrell,
Radona R Boutte,
Randy L Clarida,
Rashard A Knight,
Rashonda N Rucker,
Reba A Gates,
Richard L Garcia,
Robert P Neligan,
Robert W Turner,
Robin N Goins,
Sandra I Gaul,
Sandra R Saunders,
Shayla G Turnipseed,
Simone M Edmonson,
Smith,
Sonya M Edmonds,
State Agency,
Tamika D Cathey,
Theresa L Stewart,
Tracy R Ball,
Tyrico K English,
Walker,
Watson,
Weedb,
Williams,
Young Kim,
Zachary J Conlin
Tallman's Documents
Publish Date | Document Type | Title |
---|---|---|
January, 2000 | FDA 483 | Bestco, LLC - Form 483, 2000-01-11 |
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](https://redica.com/document-store/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