FDA Investigator Patricia D Stahnke
Patricia D Stahnke has conducted inspections on 9 sites in 4 countries as of 02 Jul 2015. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
9
Last Inspection Date:
02 Jul 2015
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United Kingdom of Great Britain and Northern Ireland,
Belgium,
Italy,
United States of America
FDA Investigators that have inspected at least one site in common with Patricia D Stahnke:
Alan P Kurtzberg,
Anastasia G Lolas,
Anissa M Cheung,
Brenda W Uratani, PhD,
Brooke K Higgins,
Bryce A Hammer,
Burnell M Henry,
Caroline H Le,
Catherine J Laufmann,
Cheryl A Clausen,
Christine L Williams,
Courtney R Bratina,
David A Gonzalez,
David J Gomes,
David M Beltran,
Douglas C Kovacs,
Dr. Barbara D Paul, PhD,
Edith M Gonzalez,
Edwin Melendez,
Elizabeth D Gonzales,
Erika V Butler,
Felix Maldonado,
Genoula K Ryan,
Gerald B Seaborn, Jr,
Ginger M Sykes,
Gwyn G Dickinson,
Haroon Vohra (NMI),
Helen B Ricalde,
Isabel Y Espinosa,
Ivis L Negron,
James C Maclaughlin,
Jamie L Dion,
Jonathan R Campos,
Julie D Bringger,
Justin A Boyd,
Kathy Lee,
Kevin A Gonzalez,
Kham Phommachanh,
Kimberley A Hoefen,
Larisa E Pavlick,
Larry K Austin,
Laura Fontan, MS,
Lewis K Antwi,
Libia M Lugo,
Linda F Murphy,
Linda M Cheny,
Marcus F Yambot,
Margarita Santiago,
Marion Michaelis,
Marvin D Jones,
Mary E Farbman, PhD,
Matthew R Dionne,
Megan A Haggerty,
Michael E Maselli,
Michael R Goga,
Mihaly S Ligmond,
Mra Davism,
Mra Mcculloughj,
Mra Munizn,
Nancy G Schmidt,
Omotunde O Osunsanmi,
Pal S Mayasandra,
Patricia A Maestas,
Paul L Figarole, Jr,
Ravichandran Veerasamy, PhD,
Rebecca E Dombrowski,
Regina T Brown,
Richard Ledwidge (nmi), PhD,
Robert J Burger,
Rose Xu,
Rowena S Nguyen,
Sangeeta M Khurana, PhD,
Santiago Gallardo Johnson,
Satheesh Thomas,
Sharon K Thoma, PharmD,
Sixto M Mercado Rios,
Stephen D Brown,
Steven C Madzo,
Steven P Donald,
Susan M Jackson,
Susan T Hadman,
Tamara L Setzer,
Tammara A Stephens,
Theressa B Smith,
Wayne E Seifert,
Zachary A Bogorad,
Zachary L Miller,
Zachary L Stamm,
Zhong Li, PhD,
Zhongren Wu
Patricia D Stahnke's Documents
Publish Date | Document Type | Title |
---|---|---|
December, 2009 | FDA 483 | TOLMAR, INC - Form 483, 2009-12-11 |
July, 2014 | FDA 483 | FUJIFILM Diosynth Biotechnologies UK Ltd - Form 483, 2014-07-11 |
July, 2015 | FDA 483 | SmithKline Beecham Ltd - Form 483, 2015-07-10 |
June, 2015 | FDA 483 | Pfizer Manufacturing Belgium NV - Form 483, 2015-06-30 |
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