FDA Investigator Jean M Mulinde, MD
Jean M Mulinde, MD has conducted inspections on 8 sites in 3 countries as of 28 Jan 2019. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
8
Last Inspection Date:
28 Jan 2019
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Cayman Islands,
United Kingdom of Great Britain and Northern Ireland
FDA Investigators that have inspected at least one site in common with Jean M Mulinde, MD:
Addam S Reynolds,
Ana P Barido,
Annet R Rajan,
Anthony J Donato,
Barbara D Wright,
Bei Yu,
Brandon L Mariner,
Byungja E Marciante,
Charles R Bonapace, PhD,
Christina P Burkhart,
Craig A Garmendia,
Cynthia F Kleppinger, MD,
Daniel J Grabicki,
Daniel J Roberts,
David L Chon,
Dawn L Wydner,
Douglas C Kovacs,
Ekaterina Allen,
Emest F Bizjak,
Frederick F Razzaghi,
Guerlain Ulysse,
Hector Jcolon Torres,
James R Birkenstamm,
Jazmine N Brown,
Jenn W Sellers,
John Dan,
Jonee J Mearns,
Joy Rkozlowski Klena,
Justine Tomasso,
Kelli F Dobilas,
Kristy A Zielny,
Lauren Iacono Connors, PhD,
Lee Hong Pai Scherf,
Liming Zhang,
Lori S Lawless,
Marea K Harmon,
Michael R Klapal,
Michael Serrano,
Mra Mcculloughj,
Nancy L Rolli,
Nebil A Oumer,
Nina Yang,
Paul L Bellamy,
Peter R Lenahan,
Robin R Waller,
Shirley S Wen,
Walden H Lee,
Yangmin Ning
Jean M Mulinde, MD's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| June, 2017 | EIR | Rho, Inc. - EIR, 2017-06-30 |
| December, 2015 | EIR | Eisai, Inc. - EIR, 2015-12-09 |
| December, 2015 | FDA 483 Response | Eisai, Inc. - Form 483R, 2015-12-18 |
| June, 2017 | FDA 483 | Rho, Inc. - Form 483, 2017-06-30 |
| June, 2008 | FDA 483 | Johnson & Johnson Pharmaceutical Research & Development, LLC - Form 483, 2008-06-12 |
| February, 2018 | FDA 483 | Eisai, Inc. - Form 483, 2018-02-16 |
| June, 2008 | EIR | Johnson & Johnson Pharmaceutical Research & Development, LLC - EIR, 2008-06-12 |
| December, 2015 | FDA 483 | Eisai, Inc. - Form 483, 2015-12-09 |
| August, 2016 | FDA 483 | Merck Sharp & Dohme LLC - Form 483, 2016-08-26 |
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