FDA Investigator Julia Ventura
Julia Ventura has conducted inspections on 248 sites in 3 countries as of 05 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
248
Last Inspection Date:
05 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Netherlands,
Greece
FDA Investigators that have inspected at least one site in common with Julia Ventura:
Alexandra B Pitkin,
Alicia Aborg Borm,
Amy R Glynn,
Ana Djurdjevic,
Anastasia M Shields,
Anthony G Emerson,
April P Shaw,
Arie R Dyk,
Arnold C Shih,
Ashley S Ertzman,
Barbara J Rincon,
Bichsa T Tran,
Binh T Nguyen,
Breena L D'ambrogi,
Brian A Perkins,
Brian P Putz,
Bruce R Burrell,
Bush,
Carla J Lundi,
Carrie A Hughes,
Caryn M Mcnab,
Cathleen A Carr Sharpe,
Celena Ngo,
Christopher R Czajka,
Clint R Van Blaricom,
Crystal A Harlan,
Cynthia A Myers,
Darrin E Davis,
David Serrano,
David Y Hernandez,
Davis,
Deborah A Greco,
Debra J Fracassa,
Dejon N Harris,
Dennis N Hoang,
Dennis R Hudson,
Desiree C Iya,
Devon M Shoop,
Diana L Ayala,
Dirk L Lincoln,
Don A Brunssen,
Donald B Mckechnie,
Douglas J Scott,
Eileen T Dupont,
Ellen N Stewart,
Eric C Milstead,
Erica R Mahone,
Falina N Hutchinson,
Gabriel Craig,
Garciam,
Garrad R Poole,
Glenn S Quintanilla,
Gordon T Wales,
Greg K Keshishyan,
Gulshan R Anand,
Hanna L Potter,
Henry E Carrillo,
Herminio C Francisco,
Hughes,
Hunter M Vice,
Indigo A Doll,
Jacobitz,
Jake T Lane,
James A Barreto,
James D Hildreth,
Jean C Colon Lopez,
Jeannine K Wooten,
Jeff A Gard,
Jeff M Uriarte,
Jennifer M Gogley,
Jessica B Clark,
Jinnie Kokiatkulkij,
Joel D Hustedt,
John A Gonzalez,
John W Banks,
Joie A Riehle,
Jolanna A Norton,
Jonathan K Dare,
Jonetta I Collins,
Joseph M Allen,
Joseph M Willems,
Joseph R Haynes,
Joseph S Fanelli,
Judy C Nepsa,
Julian C Hanson,
Ka L Wong,
Katharine Chan,
Kathryn A Krentz,
Kelly S Mammen,
Kelsey M Bishop,
Kelvin X Sanders,
Kevin Lee,
Kevin T Gerrity,
Kham Phommachanh,
Kim Lthomas Cruse,
Kimberly M Lichter,
Krista K Petersen,
Lacresha Menifee,
Lam,
Lance W Bohm,
Lanita F Kelley,
Lesley A Swanson,
Lester O Boian,
Leya A Grosch,
Ligia M Cline,
Lilly O Barton,
Lin Liu,
Ling Yu L Liu,
Lopez,
Loretta J Jordan,
Lori J Jennings,
Lucas B Leake,
Mageet,
Mai X Huynh,
Marcus A Goshen,
Marcus F Yambot,
Margo C Jones,
Mark C Saale,
Mark E Imsland,
Maurice M Sheehan,
Michael D Garcia,
Michael F Schuette,
Michelle J Hines,
Mikel T Wright,
Muoi N Hoang,
Myers,
Nancy E Byerly,
Narahi J Alvarez Alcazar,
Nathan R Moon,
Naveen B Walker,
Nianna C Burns,
Nicholas L Hunt,
Pamela Y Lee,
Phal K Chhun,
Phillip J Sample,
Phillip L Toy,
Rachelle M Deskins,
Richard T Jensen,
Richard W Tubb,
Richmond K Yip,
Robert A Williams,
Robert D Tollefsen,
Rocco C Black,
Rochelle A Rolnik,
Rocio Guzman Velazquez,
Roger J Adams,
Ryan M Solberg,
Sandra A Boyd,
Sandra K Wangen,
Sara Jdent Acosta,
Scott J Matsuda,
Sean P Desbrow,
Sharon S Ho,
Shaun M Olson,
Shelly M King,
Sonya L Karsik, RAC,
Sparky L Bartee,
Steven E Porter, Jr,
Sunny R Muir,
Susan K Bain,
Sydney S Taylor,
Tammy Vasquez Hancock,
Tawny L Colling,
Thomas W Gordon,
Timothy D Evans,
Timothy P Lafave,
Timothy T Kapsala,
Tomanik'e C Banks,
Tony J Wu,
Tracy K Li,
Truong Xuan Nguyen (Andy),
Trushani T Desai,
Tuan D Tran,
Uttaniti Limchumroon (Tom),
Vanessa R Muller,
Victor H Loo,
Vitaliy N Guyvan,
Walden H Lee,
Willemsj,
William C Hughes,
Yen Tso Kuo,
Zachary A Bogorad
Julia Ventura's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2011 | FDA 483 | Global Product Management, Inc. - Form 483, 2011-03-07 |
December, 2022 | FDA 483 | CHS Animal Nutrition - Great Falls - Form 483, 2022-12-19 |
March, 2012 | FDA 483 | Bluefield Associates, Inc. - Form 483, 2012-03-07 |
January, 2023 | FDA 483 | Hillside Dairy LLC - Form 483, 2023-01-26 |
September, 2022 | FDA 483 Response | Arrow Reliance Inc - Form 483R, 2022-09-30 |
April, 2011 | FDA 483 | Jongs Poultry Farm, Inc. - Form 483, 2011-04-08 |
September, 2022 | FDA 483 | Arrow Reliance Inc - Form 483, 2022-09-30 |
July, 2023 | FDA 483 | Moo Mountain Milk Inc - Form 483, 2023-07-13 |
April, 2023 | FDA 483 | Land View Inc - Form 483, 2023-04-28 |
September, 2024 | FDA 483 | Arrow Reliance Inc - Form 483, 2024-09-18 |
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