FDA Investigator Rosario D'costa
Rosario D'costa has conducted inspections on 4 sites in 1 countries as of 22 Jul 2003. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
4
Last Inspection Date:
22 Jul 2003
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Rosario D'costa:
Azeezat M Lawal,
Barbara Jwilimczyk Macri,
CDR Ileana Barreto Pettit,
Chhagan Tele,
Christian F Gomez Lugo,
Christina K Theodorou,
Christos G Tsingelis,
Dacia E Quick,
Daniel J Grabicki,
Daryl A Dewoskin,
David A Oluwo,
Devon Jenkins,
Dr. Dominick Roselle,
Edward H Maticka,
Gregory W Smith,
Ivan E Reyes,
Jennifer A Robinson,
Jennifer Lalama,
Jessica L Pressley,
Jogy George,
Jonathan G Matrisciano,
Jose Perez Soto,
Joshua J Silvestri,
Joy Rkozlowski Klena,
Justin A Boyd,
Justine Tomasso,
Karen E D'orazio,
Kayla V Sprague,
Kristy E Zuroski,
Krystyna M Kitson,
LCDR Michael H Tollon,
Loretta Nemchik,
Lori M Newman,
Lourdes Andujar,
LT Kimberly M Hull,
Luis Mburgos Medero,
Lynne Ensor,
Marea K Harmon,
Margaret M Sands,
Marie A Fadden,
Melissa I Michurski,
Monica Cburgos Garcia,
Moraima Jramos Valle,
Nancy M Espinal,
Nicole E Knowlton,
Paul L Bellamy,
Paul L Figarole, Jr,
Rochelle L Cross,
Russell J Glapion,
Saleem A Akhtar,
Salvatore N Randazzo,
Sean R Marcsisin,
Sharon K Thoma, PharmD,
Tamil Arasu, PhD,
Yoriann M Cabrera Bartolomei,
Yvesna C Blaise
Rosario D'costa's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2003 | FDA 483 | Cima Labs, Inc. - Form 483, 2003-08-01 |
July, 2000 | FDA 483 | Catalent Pharma Solutions, LLC - Form 483, 2000-07-21 |
August, 2003 | EIR | Cima Labs, Inc. - EIR, 2003-08-01 |
August, 2003 | EIR | Cima Labs, Inc. - EIR, 2003-08-01 |
July, 2000 | FDA 483 Response | Catalent Pharma Solutions, LLC - Form 483R, 2000-08-01 |
July, 2000 | EIR | Catalent Pharma Solutions, LLC - EIR, 2000-07-21 |
August, 2003 | FDA 483 | Cima Labs, Inc. - Form 483, 2003-08-01 |
April, 2003 | EIR | Hikma Pharmaceuticals USA Inc. - EIR, 2003-04-29 |
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