FDA Investigator Edwardstine J Reese
Edwardstine J Reese has conducted inspections on 163 sites in 4 countries as of 26 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
163
Last Inspection Date:
26 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
India,
China,
Italy
FDA Investigators that have inspected at least one site in common with Edwardstine J Reese:
Alexandra A Carrico,
Amina Bashir,
Ana E Morales,
Ana L Kewes,
Anthony R Ronga,
Antoinette L Chancey,
Antonio M Hampton,
Armando Morales,
Ashley L Reiber,
Ashley R Karns,
Audrey Dela Cruz,
Ava M Bowman,
Beverley A Phillips,
Bing Lin,
Brandi N Mcgrady,
Brentley S Collins,
Brian D Nicholson,
Brian J Davis,
Brian M Campbell,
Brian P Emanuel,
Brian P Hendrickson,
Brian R Yaun,
Brittany R Laymon,
Bruce H Mccullough,
Calvin K Cook,
Cambria Cook Krueger,
Carl A Huffman, III,
Carrie L Doupnik,
Catherine D Djordjevic,
Cathie S Marshall,
Chad J Whitwell,
Charles E Frelix,
Charles M Spyr,
Charlie P Booker,
Chase S Baldwin,
Chelsea J Snider,
Clotia Cabbey Mensah,
Corrine M Carter,
Craig P Seaborn,
Daniel B Arrecis,
Daniel J Brown,
Daniel J Gorski,
Danny Tuntevski,
Dariusz Galezowski,
Darren S Morgan,
David A Paterson,
David P Moorhead,
Dawnna D Brown,
Deanna L Lampley,
Debra I Love,
Dell S Moller,
Dennis R Downer,
Donna K Speer,
Dorathy M Eischen,
Douglas C Kovacs,
Elizabeth L Holmes,
Elizabeth P Mayer,
Emest F Bizjak,
Eric S Pittman,
Erin M Miller,
Fernando C Martinez,
Freed A Sharif,
Hans T Meyers,
Hassan Ali,
Ifueko Osemwota,
James E Roberts,
James P Duggan,
James T Karpus,
James W Plucinski,
Jayne E Holcomb,
Jeanne J Chiu,
Jennifer A D'angelo,
Jennifer A Downie,
Jennifer C Johnson,
Jennifer L Johnson,
Jennifer L Mecher,
Jennifer M Heitz,
Jennifer R Johnson,
Jesse A Vazquez,
Jessica L Burley,
Jocelyn C Turner,
John M Seale,
John N Woodall,
Joie A Navarrete,
Joseph D Cooper,
Joseph R Strelnik,
Joseph T Dougherty,
Joshua M Adams,
Kayla D Smith,
Kelley L Clark,
Kelli L Wilkinson,
Kelsey L Vansickle,
Kimberly A Joseph,
Kirk A Dymbrowski,
Kristen E Szenderski,
Kristina Nastovski,
L'oreal F Walker,
Larry K Austin,
Latoya A Griffith,
Laura A Grumenfelder,
Lauren A Crivellone,
Lauren E Burke,
Lauren E Sexton,
Laurie A Haxel,
Linda S Jozefiak,
Logan M Ebeling,
Mancia R Walker,
Marcia A Worley,
Margaret N Klug,
Margaret N Persich,
Maria Diaz,
Mark E Baldwin,
Mark G Peterson,
Mark I Kaspar,
Martin R Vowell,
Matt D Suedkamp,
Matthew J Gretkierewicz,
Matthew R Buenconsejo,
Meisha Waters,
Michael E Campbell,
Michelle L Jones,
Misty D Harvey,
Mobin A Tawakkul,
Nantie,
Natalie A Mickelsen, DVM,
Neal D Singletary, PhD,
Nelson A Rodriguez,
Nicole J Clausen,
Owens,
Pablo Alcantara,
Patrick B Cummings,
Patrick E Gainer,
Paula P Demichael,
Peyton B Greenwood,
Phung Thien Nguyen,
Pifer,
Rafeeq A Habeeb,
Randy D Baxter,
Raquel L Coleman,
Renee L Anderson,
Robert D Ogan,
Robert M Barbosa,
Roberta W Cunningham,
Roger A Hartman,
Roger J Adams,
Ronald P Boyce,
Rosemary Wood Sexton,
Roshni J Patel,
Russell K Riley,
Said H Muse,
Sarah Nwandiuko,
Shana L Williams,
Shelton L Stribling,
Stefen D Mcmillan,
Sullan,
Susan D Yuscius,
Susan M Taylor,
Susan W Ciani,
Tamayo C Barnes,
Tara C Alcazar,
Tara M Carolfi,
Tarsha T Mcclendon,
Theodore N Sietsema,
Thomas J Hudson,
Thomas J Prigge,
Thomas W Nojek,
Thunder N Dunkijacobs,
Thursaml,
Todd M Stankewicz,
Tonnie L Carter,
Travis S Bradley,
Twana R Chandler,
Uruaku A Obasi,
Vera M Anderson,
Vesa Vuniqi,
Wayne W Grundstrom,
William D Sherman,
William G Nelson,
William R Weissinger
Edwardstine J Reese's Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2019 | FDA 483 Response | Caito Foods LLC. - Form 483R, 2019-07-23 |
December, 2018 | FDA 483 | CONAGRA BRANDS CORPORATION - Form 483, 2018-12-18 |
April, 2017 | FDA 483 | Tate & Lyle Ingredients Americas, LLC - Form 483, 2017-04-19 |
February, 2019 | EIR | Strebor Specialties, LLC. - EIR, 2019-02-13 |
July, 2019 | FDA 483 | Caito Foods LLC. - Form 483, 2019-07-01 |
November, 2021 | EIR | The Elderberry Co., LLC - EIR, 2021-11-03 |
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