FDA Investigator Haroon Vohra (NMI)
Haroon Vohra (NMI) has conducted inspections on 29 sites in 1 countries as of 13 Feb 2018. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
29
Last Inspection Date:
13 Feb 2018
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 Haroon Vohra (NMI):
Alan P Kurtzberg,
Alejandro Rodriguez,
Alexandra B Pitkin,
Amalia C Himaya,
Andrea S Heise,
Andrew M Kolenc,
Anita Narula, PhD,
Arie C Menachem,
Arsen Karapetyan,
Ashley M Caputo,
Barry Cherney, PhD,
Betty Kay Baxter,
Bichsa T Tran,
Bo Chi, PhD,
Brandon K Lawson,
Brien C Fox,
Bryce A Hammer,
Carla J Lundi,
Carolina D Vasquez,
Caroline H Le,
Caryn M Mcnab,
Chani Broner, PhD,
Cheron M Portee,
Christina C Santos,
Christina V Santos,
Christine I Shaw,
Christine L Williams,
Christine R Casey,
Crystal Monroy,
Cynthia Jim, CSO,
Daniel Pst Laurent,
Daniel W Cline,
Darrin E Davis,
David A Gonzalez,
Davinna Ligons, PhD,
Daynia L Lashaway,
Diane Cvan Leeuwen,
Doan T Nguyen, PharmD,
Donna Ltartaglino Besone,
Edith M Gonzalez,
Elaine G Stewart,
Erik W Burrows,
Erika V Butler,
Esther C Broner, PhD,
Farhana Khan,
Frances Namuswe, PhD,
Frank L Cordova,
Frederick L Fricke,
Genoula K Ryan,
Gerard T Schneider,
Ginger M Sykes,
Grace E Mcnally,
Greg K Keshishyan,
Gwyn G Dickinson,
Haley H Seymour,
Hanna L Potter,
Hasan A Irier, PhD,
Iris C Macinnes,
Isabel Y Espinosa,
Jai P Singh,
James R Fleckenstein,
Jamie L Dion,
Janet Pulver,
Jee Chung, PhD,
Jeffrey P Raimondi,
Jennifer Gogley,
Jennifer M Gogley,
Jennifer R Mathern,
Jessica M Ector,
Joel Welch, PhD,
Joey V Quitania,
John A Gonzalez,
John R Myung,
Junho Pak,
Ka L Wong,
Karen A Wolnik,
Karen G Hirshfield,
Karen Wolnik,
Katherine Szestypalow,
Kathleen R Jones, PhD,
Kathryn M Mogen,
Kelvin Cheung,
Kelvin X Sanders,
Kendra A Biddick,
Kent C Faul,
Kim Lthomas Cruse,
Kimberley A Hoefen,
Kristen E Szenderski,
Lance A Finnical,
Larisa E Pavlick,
Laura B Kennedy,
Laura Fontan, MS,
Leonard H Lavi,
Linda F Murphy,
Linda M Cheny,
Marcia B Williams,
Marcus F Yambot,
Mariza M Jafary,
Marlene G Swider,
Matthew A Johnson,
Matthew R Dionne,
Maxyne T Lam,
Meaghan M Rabideau,
Michael A Charles,
Michael E Maselli,
Michael J Kuchta,
Michael Kuchta,
Michael R Goga,
Michael S Araneta,
Michelle A Marsh,
Mihaly S Ligmond,
Mohsen Rajabi Abhari, FDA,
Morie Alpha,
Nancy G Schmidt,
Nathan M Jornod,
Nathan R Moon,
Nayan J Patel,
Nicholas Obiri, PhD,
Nicola M Fenty Stewart,
Omotunde O Osunsanmi,
Patricia A Brown,
Patricia A Cortez,
Patricia A Maestas,
Patricia Brown,
Patricia D Stahnke,
Paul J Teitell,
Peter S Diak,
Prabhu P Raju,
Ramesh Raghavachari,
Rebecca H Lee,
Rebecca Rodriguez,
Richmond K Yip,
Ricki A Chase,
Robert D Tollefsen,
Robert Darius,
Robert J Burger,
Robert Sharpnack,
Roger F Zabinski,
Roger L Farmer,
Rona Leblanc, PhD,
Ronald L Koller,
Ronda Leblanc,
S Lori Brown, PhD MPH,
Saied A Asbagh,
Samantha E Rafferty,
Santiago Gallardo Johnson,
Sarah Arden,
Scott R Nichols, PhD,
Secrist,
Sheila Alaghemand,
Shererk,
Sidney B Priesmeyer,
Siobhan A Gallagher,
Sonia R Peterson,
Stacie A Woods,
Stanley Au,
Steve P Yost,
Steve Y Rhieu, PhD,
Steven Fong, MS, PhD,
Sundy V Sedwick,
Taichun Qin, PhD,
Tamika White,
Tara L Breckenridge,
Tara L Greene,
Tenzin Jangchup,
Teresa I Navas,
Terri L Dodds,
Thai T Duong,
Thao T Kwan,
Thao X Tran,
Theressa B Smith,
Uttaniti Limchumroon (Tom),
Walden H Lee,
Yumi J Hiramine,
Yvonne C Wilkes,
Zachary A Bogorad,
Zachary L Miller,
Zachary L Stamm,
Zhong Li, PhD
Haroon Vohra (NMI)'s Documents
Publish Date | Document Type | Title |
---|---|---|
February, 2018 | FDA 483 | Wallsburg Farms Inc. - Form 483, 2018-02-16 |
June, 2017 | FDA 483 | Safeway, Inc. - Form 483, 2017-06-12 |
December, 2016 | EIR | Curia New Mexico, LLC - EIR, 2016-12-07 |
September, 2017 | FDA 483 | Ultradent Products, Inc. - Form 483, 2017-09-15 |
December, 2016 | FDA 483 | Curia New Mexico, LLC - Form 483, 2016-12-07 |
January, 2018 | FDA 483 | College Pharmacy, Inc. - Form 483, 2018-01-17 |
April, 2017 | EIR | USANA Health Sciences, Inc. - EIR, 2017-04-21 |
October, 2017 | EIR | New Generation Wellness - EIR, 2017-10-27 |
December, 2017 | EIR | PureTek Corporation - EIR, 2017-12-15 |
May, 2016 | FDA 483 | Corden Pharma Boulder, Inc. - Form 483, 2016-05-02 |
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