FDA Investigator Rodney T Allnutt
Rodney T Allnutt has conducted inspections on 4 sites in 1 countries as of 07 Jun 2004. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
4
Last Inspection Date:
07 Jun 2004
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 Rodney T Allnutt:
Allen F Hall,
Allen Lou,
Barbara M Frazier,
Byungja E Marciante,
Charles J Chacko,
Cheryl A Grandinetti,
Christina N Maurino,
Deborah B Nixon,
Denise M Visco, Investigator,
Douglas C Kovacs,
Emmanuel Jramos Maldonado,
Eric Rothschild,
Erin D Mccaffery,
Ernest A Clausnitzer,
George Pyramides,
Guerlain Ulysse,
Iris C Macinnes,
James R Fleckenstein,
Jean M Kelahan,
Joan A Loreng,
Karen E D'orazio,
Kassa Ayalew, MD,
Kirtida Patel,
Lata C Mathew, PhD,
Leonard H Lavi,
Liatte Kreuger, PharmD,
Lisa Harlan,
Matthew A Spataro,
Mayar M Mussa,
Melissa T Roy,
Michael Serrano,
Nina Yang,
Paul L Bellamy,
Peter R Lenahan,
Regina T Brown,
Robert Jennings,
Shari H Shambaugh,
Shari J Hamilton,
Stephanie E Hubbard,
Stephanie T Durso,
Tonia F Bernard,
Tyanna N Hadley,
Wr Bowman,
Yvesna C Blaise
Rodney T Allnutt's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| May, 2003 | EIR | American Cardiovascular Res Ins - EIR, 2003-05-09 |
| February, 2001 | FDA 483 | Mentor Worldwide LLC - Form 483, 2001-12-06 |
| June, 2004 | FDA 483 | Novartis Pharmaceuticals Corporation - Form 483, 2004-06-10 |
| June, 2004 | EIR | Novartis Pharmaceuticals Corporation - EIR, 2004-06-10 |
| August, 2000 | FDA 483 | University of South Florida-Division of Comparative Medicine - Form 483, 2000-08-04 |
| May, 2003 | FDA 483 | American Cardiovascular Res Ins - Form 483, 2003-05-09 |
| August, 2000 | EIR | University of South Florida-Division of Comparative Medicine - EIR, 2000-08-04 |
| May, 2003 | FDA 483 Response | American Cardiovascular Res Ins - Form 483R, 2003-06-06 |
| June, 2004 | FDA 483 Response | Novartis Pharmaceuticals Corporation - Form 483R, 2004-07-02 |
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