FDA Investigator Rebeca M Melendez
Rebeca M Melendez has conducted inspections on 8 sites in 1 countries as of 23 May 2017. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
8
Last Inspection Date:
23 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 Rebeca M Melendez:
Abigail A Auster,
Adalberto Cajigas,
Adaliz Santaliz Cruz,
Alan A Rivera,
Angelica M Hernandez,
Ann L Demarco,
Annette Melendez,
Ariel Cruz Figueroa,
Arlene M Badillo,
Arwa S El Hagrasy,
Binh T Nguyen,
Brenda Rivera,
Brian J Ryan,
Carlos A Medina,
Christina Capacci Daniel, PhD,
Dayna I Martinez,
Dennis Cantellops Paite,
Donna Christner,
Edwin Martinez,
German Rivera,
Iraida Ortiz,
Ivis L Negron,
Javier O Vega,
Jorge L Gonzalez,
Jorge L Guadalupe,
Jose A Lopez,
Jose A Moreno,
Jose Acruz Gonzalez,
José E Meléndez,
Jose F Pedro,
Jose Martinez, Jr,
Jose R Lopez,
Jose Velez,
Juan Rjimenez Garcia,
Laura E Garcia,
Laurimer Kuilan Torres,
Libia M Lugo,
Lisa M Lopez,
Lourdes Andujar,
Marian E Ramirez,
Michelle Yclark Stuart,
Miguel A Martinez Perez,
Miguel Hernandez Sanchez,
Min Tang,
Muralidhara B Gavini, PhD,
Myriam M Sosa,
Noreen Muñiz,
Pablo Feliciano,
Rafael E Cruz,
Rafael Nevarez Nieves,
Ramon A Hernandez,
Raquel Gonzalez Rivera,
Rebecca Parrilla,
Rebecca Rodriguez,
Regina T Brown,
Sharmista Chatterjee,
Sixto M Mercado Rios,
Steven B Barber,
Thomas J Arista,
Vilmary Negron Rodriguez,
Wanda J Torres
Rebeca M Melendez's Documents
Publish Date | Document Type | Title |
---|---|---|
June, 2017 | FDA 483 | Neolpharma, Inc. - Form 483, 2017-06-07 |
March, 2009 | FDA 483 | Pfizer Pharmaceuticals LLC - Form 483, 2009-03-19 |
July, 2016 | FDA 483 | AbbVie Ltd - Form 483, 2016-07-29 |
June, 2006 | EIR | Janssen Ortho LLC - EIR, 2006-06-15 |
June, 2006 | FDA 483 | Ivax Pharmaceuticals, Inc. - Form 483, 2006-06-02 |
June, 2017 | EIR | Neolpharma, Inc. - EIR, 2017-06-07 |
March, 2003 | FDA 483 | Bristol-Myers Squibb Holdings Pharma, Ltd. Liability Company - Form 483, 2003-03-13 |
March, 2003 | EIR | Bristol-Myers Squibb Holdings Pharma, Ltd. Liability Company - EIR, 2003-03-13 |
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