FDA Investigator Michael C Kennedy, PhD
Michael C Kennedy, PhD has conducted inspections on 9 sites in 6 countries as of 30 Jul 2018. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
9
Last Inspection Date:
30 Jul 2018
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
France,
Netherlands,
Mexico,
United States of America,
Korea (Republic of),
Sweden
FDA Investigators that have inspected at least one site in common with Michael C Kennedy, PhD:
Alan L Truong,
Andrey Sarafanov, PhD,
Anthony F Lorenzo,
Barbara T Carmichael,
Burnell M Henry,
CDR Cecily Jones,
CDR Donald Ertel,
Christian D Lynch (CDL),
Cynthia Jim, CSO,
Deborah M Trout,
Dusty F Snoeberg,
Eileen A Liu,
Felice D'agnillo, PhD,
Gregory Price,
Hector A Carrero,
Holly Brevig,
Ivan E Reyes,
J David Doleski,
Jacqueline Mdiaz Albertini,
Janet L Bowen,
Jennifer L Reed,
Jie He,
Joan A Loreng,
Julie D Bringger,
Justin A Boyd,
LCDR Debra Emerson,
Lily Y Koo,
Lori Peters,
Malgorzata G Norton, PhD,
Margaret Norton,
Michael J Vardon,
Michele L Forster, PhD,
Mihaly S Ligmond,
Mikhail V Ovanesov, PhD,
Nancy Kirschbaum, PhD,
Nancy T Waites,
Nicole M Li,
Nimmy Mathews,
Obinna R Echeozo,
Olga Simakova, PhD,
Omotunde O Osunsanmi,
Pankaj H Amin,
Prabhu P Raju,
Randa Melhem, PhD,
Rebecca K Olin,
Richard Heath Coats,
Robert Jennings,
Robert W Fisher,
Roger F Zabinski,
Rose Ashley,
Scott T Ballard,
Sheri L Stephenson,
Simone E Pitts,
Susan M Jackson,
Susan M Turcovski,
Xiuju Lu,
Yiping Jia,
Yonggang Wang, PhD,
Yvesna C Blaise,
Ze Peng
Michael C Kennedy, PhD's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| June, 2016 | FDA 483 | GC Biopharma Corp_Ochang Plant - Form 483, 2016-06-21 |
| March, 2018 | FDA 483 | Baxalta US Inc. - Form 483, 2018-03-02 |
| June, 2008 | FDA 483 | ADMA Biologics, Inc - Form 483, 2008-06-11 |
| May, 2012 | FDA 483 | ADMA Biologics, Inc - Form 483, 2012-05-17 |
| August, 2018 | FDA 483 | Laboratorios Silanes, S.A. de C.V. - Form 483, 2018-08-03 |
| January, 2014 | FDA 483 | Instituto Bioclon S.A. de C.V. - Form 483, 2014-01-23 |
| January, 2012 | FDA 483 | Octapharma AB - Form 483, 2012-01-19 |
| May, 2018 | FDA 483 | Octapharma S.A.S. - Form 483, 2018-05-25 |
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