FDA Investigator Jose A Moreno
Jose A Moreno has conducted inspections on 13 sites in 1 countries as of 15 May 2017. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
13
Last Inspection Date:
15 May 2017
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
Puerto Rico
FDA Investigators that have inspected at least one site in common with Jose A Moreno:
Adalberto Cajigas,
Alicia M Mozzachio,
Anastasia M Shields,
Angelica M Hernandez,
Annette Melendez,
Ariel Cruz Figueroa,
Arlene M Badillo,
Arwa S El Hagrasy,
Binh T Nguyen,
Carlos A Medina,
Cassandra L Abellard,
CDR Ileana Barreto Pettit,
Christina Capacci Daniel, PhD,
Colleen F Hoyt,
Dayna I Martinez,
Dennis Cantellops Paite,
Donna Christner,
Dr. Carmelo Rosa,
Edwin Martinez,
Enrique Galan,
Frederick L Fricke,
German Rivera,
Hector Jcolon Torres,
Iraida Ortiz,
Ivis L Negron,
Joan M Cantellops Figueroa,
Joe X Phillips,
Jorge L Gonzalez,
Jorge L Guadalupe,
Jorge L Lajara,
Jose A Lopez,
Jose Acruz Gonzalez,
José E Meléndez,
Jose F Pedro,
Jose R Lopez,
Jose Velez,
Laiza V Garcia,
Laura E Garcia,
Laurimer Kuilan Torres,
Libia M Lugo,
Lisa M Lopez,
Lourdes Andujar,
LT Rafael Gonzalez,
Luis Soto Lopez,
Marianela Aponte Cruz,
Maribel V Juarbe,
Marie T Falcone,
Marta E Gonzalez,
Michael R Klapal,
Miguel A Martinez Perez,
Milva E Melendez Perales,
Myriam M Sosa,
Neisa M Alonso,
Nimmy Mathews,
Noreen Muñiz,
Pablo Feliciano,
Patrick C Klotzbuecher,
Rafael Nevarez Nieves,
Ramon A Hernandez,
Randy L Clarida,
Raquel Gonzalez Rivera,
Rebeca M Melendez,
Rebecca Parrilla,
Rebecca Rodriguez,
Scott T Ballard,
Sharmista Chatterjee,
Sixto M Mercado Rios,
Stacie A Woods,
Steven B Barber,
Victor S Pacheco,
Vilmary Negron Rodriguez,
Viviana Matta,
Wanda J Torres
Jose A Moreno's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| September, 2003 | EIR | IPR Pharmaceuticals, Inc - EIR, 2003-09-29 |
| May, 2017 | FDA 483 | Janssen Ortho LLC - Form 483, 2017-05-26 |
| May, 2010 | FDA 483 | Patheon Puerto Rico, Inc. - Form 483, 2010-05-04 |
| May, 2017 | EIR | Janssen Ortho LLC - EIR, 2017-05-26 |
| July, 2008 | FDA 483 | Fenwal International, Inc. - Form 483, 2008-07-15 |
| January, 2006 | FDA 483 | Smithkline Beecham (Cork) Inc. - Form 483, 2006-01-23 |
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