FDA Investigator David T Glover
David T Glover has conducted inspections on 134 sites in 1 countries as of 30 Jun 2014. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
134
Last Inspection Date:
30 Jun 2014
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 David T Glover:
Abdur Rashid,
Adam J Williams,
Alan R Moore,
Alexis S Roberts,
Alphonso A Haupt, III,
Alysia M Salonia,
Amanda L Evanco,
Ana L Kewes,
Andrea L Williams Jones,
Anthony S Puckett,
Antoinette L Chancey,
April R Bowen,
Arlyss M Jones,
Arthur G Hurst,
Ashley Cornwell,
Babatunde D Babalola,
Billy M Battles,
Bonita S Chester,
Brenda Rivera,
Brian E Bradford,
Bruce R Burrell,
Carlos A Ortiz,
Carol J Blackwood,
Carolyn W White,
Chauncey A Stephens,
Christina H Owens,
Christina W Waters,
Christine M O'leary,
Christopher C Wilcox,
Cierra S Strong,
Claudette D Brooks,
Clinton V Giustra,
Cordelia J Brammer,
Crystal A Harlan,
D Ross Spears, PhD,
Darcy E Brillhart,
Davia K Arnold,
David R Heiar,
Davis,
Debra J Tucker,
Derek C Price,
Desiree D Clark,
Douglas Brogden B,
Douglas L Page,
Ebony W Laster,
Edward Deberry,
Emil P Wang, JD,
Ernest H Blackwood,
Esra Toussaint,
Frank Flores,
Gabriel M Guevarra,
Gabriel R Mclemore,
Gary E Coleman, Jr, REHS,
Hai Lient Phung,
Heather Akleimola Hulbert,
Hristu B Chepa,
Ibad U Khan,
Ingrid A Zambrana,
Jackie M Douglas,
James R Betz,
Janaysia N Trail,
Janet B Gray,
Janet Jones,
Janice L King,
Jason K Morgan,
Jawaid Hamid,
Jeffrey D Sheppard,
Jerry H Bridgers,
Jerry T Hunt,
Jessica Fields,
Jhakeim D Seaberry,
Jimmy O Buford,
John D Lloyd,
John E Aghadia,
Johnetta F Walters,
Johnson,
Joseph F Owens,
Juliana Falla,
Justin A Boyd,
Kara D Dobbin,
Karen L Anderson,
Katelynn J Gulya,
Katelynn J Rollins,
Kathryn A Nagy,
Katrina B Mosley Sloan,
Kenny R Robinson,
Keri U Walker,
Kerry L Edwards, III,
Kimberly Cdelk Brooks,
Kunapuli T Madhusudhan,
Lakisha N Morton,
Lareese K Thomas,
Larry K Hampton,
Laura D Cain,
Lawrence Thomas,
LCDR Audra J Lenhart,
Leroy M Anderson,
Lesley K Satterwhite,
Leslie W Gilbert,
Lillie D Witcher,
Lorenzo Jones,
Manella Crook,
Marcella D Crook,
Marie F Morin,
Marybeth Willis,
Matthew G Brown,
Mcbean,
Miaja Umaedi,
Michael M Quinn,
Michelle L Jones,
Mokhless A Ghaly,
Morrell,
Myla D Chapman,
Myoshi M Francis,
N'jere English,
Nancy E Fontaine,
Nianna C Burns,
Patricia F Hudson,
Paula J Bretz,
Penny H Mccarver,
Randy L Clarida,
Rashard A Knight,
Rashonda N Rucker,
Renee J Wilkes,
Richard L Garcia,
Robert P Neligan,
Robert Q Green,
Robert W Turner,
Robin N Goins,
Ronsha Y Hill,
Russell R Zablan,
Sally Gopaul,
Sandra I Gaul,
Sandra R Saunders,
Sarah C Pichette,
Seneca D Toms,
Sereen Gmorgan Murray,
Shayla G Turnipseed,
Sheri S Oliver,
Sherry R Dunn,
Simone E Hollis,
Simone M Edmonson,
Sondra L Phillips,
Stephanie E Hubbard,
Susan M Taylor,
Tamika D Cathey,
Thao Le,
Theresa L Stewart,
Tracy A Holloman,
Tracy R Ball,
Trang N Cox,
Tyrico K English,
Valerie L Whipp,
Vanessa E Coulter,
Veronica Fuentes, MS,
Victoria L Palmer,
Vincent M Williams,
Viviana Matta,
Wilbur G Huggins,
William K Ducloux,
Xiomara Copeland,
Xiujing L Baggett,
Young Kim
David T Glover's Documents
Publish Date | Document Type | Title |
---|---|---|
November, 2013 | EIR | Hi-Tech Pharmaceuticals Inc. - EIR, 2013-11-08 |
April, 2012 | EIR | O'Barr, Thomas MD - EIR, 2012-04-30 |
April, 2012 | FDA 483 | O'Barr, Thomas MD - Form 483, 2012-04-30 |
August, 2012 | EIR | Knex Worldwide Llc - EIR, 2012-08-07 |
November, 2012 | FDA 483 Response | Gate Gourmet #302 - Form 483R, 2012-11-30 |
December, 2012 | FDA 483 | Summit Industries - Form 483, 2012-12-13 |
August, 2011 | FDA 483 | Carolina Bone & Tissue Inc. - Form 483, 2011-08-01 |
June, 2014 | FDA 483 | Terve Sina Wellness Inc. - Form 483, 2014-06-25 |
November, 2012 | FDA 483 | Beaumont Products Inc. - Form 483, 2012-11-06 |
May, 2014 | EIR | Tobacco Rag Processors Inc - EIR, 2014-05-13 |
November, 2012 | FDA 483 | Gate Gourmet #302 - Form 483, 2012-11-30 |
October, 2010 | FDA 483 | ISE Newberry Inc. - Form 483, 2010-10-15 |
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