FDA Investigator Laurie P Norwood
Laurie P Norwood has conducted inspections on 9 sites in 5 countries as of 25 Jul 2016. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
9
Last Inspection Date:
25 Jul 2016
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Spain,
France,
United Kingdom of Great Britain and Northern Ireland,
Germany
FDA Investigators that have inspected at least one site in common with Laurie P Norwood:
Abdu Alayash,
Andrea A Branche,
Andrea George, PhD,
Angel K Sandhu,
Angela K Shen,
Anh M Lac,
Anissa M Cheung,
Anita R Michael,
Ann L Demarco,
Ann Marie Montemurro,
Barbara J Wilcox, PhD,
Brandon L Mariner,
Burnell M Henry,
Calvin B Koerner,
Carl Lee,
Carole L Jones,
Cassandra Overking,
CDR Donald Ertel,
Christian D Lynch (CDL),
Christopher R Czajka,
Craig D Zagata,
Cynthia Jim, CSO,
Cynthia L Kelley,
Daniel C Kearns,
Daniel J Roberts,
David S Cho, PhD,
Destry M Sillivan,
Dino A Fiegelstock,
Dmitriy V Volokhov, PhD,
Dr. Gang Wang, PhD,
Dr. Mark J Seaton, PhD,
Dr. Ralph M Bernstein, PhD,
Dr. Willie F Vann, PhD,
Dustin R Abaonza,
Edmund F Mrak, Jr,
Eliezar Ramos,
Ellen Huang,
Emily Shacter,
Eric L Dong, BS,
Gene D Arcy,
Gerald Feldman,
Gerald M Feldman, PhD,
Gerald Mierle,
Helen B Ricalde,
Henry K Lau,
J David Doleski,
Jacqueline Mdiaz Albertini,
James A Crim,
James E Keller, PhD,
James M Mason,
James R Evans,
Jeanne Fringer, PhD,
Jeffrey M Watson,
Jennifer L Schmidt,
Joan A Loreng,
Joan T Briones,
Joey V Quitania,
John D Finkbohner, PhD,
John F Cipollo,
John M Mcinnis,
John M Mclnnis,
Joseph George,
Joseph Kutze, PhD,
Joseph P Iser, MD,
Joshua S Hunt,
Julie D Bringger,
Justin A Boyd,
Karen M Bryerton,
Karen M Cooper,
Kevin P Foley,
Kirsten L Vadheim, PhD,
Lakisha M Williams,
Lance Mde Souza, MBA,
Larry K Austin,
Laurie B Frazier,
Laurissa S Flowers,
LCDR Jennifer H Rhyu,
Leslie D Wagner,
Lewis K Antwi,
Linda R Kuchenthal,
Linda S Mattingly,
Linda Thai,
Linh Tu,
Lisa M Parsons,
Mabel M Lee,
Maida Henesian (NMI),
Margaret Torres Vazquez,
Marian Majors, PhD,
Marie K Kinkade,
Marion Michaelis,
Marion W Nadeau,
Mariza M Jafary,
Mark A Elengold,
Marsha W Major,
Megan A Haggerty,
Michael Shanks, MS,
Michael T Cyrus,
Michele L Forster, PhD,
Michelle Rfrazier Jessen, PhD,
Mihaly S Ligmond,
Min Shanmabel Liu,
Nancy L Meade,
Nawab A Siddiqui,
Nayan J Patel,
Nicholas L Hunt,
Nicholas Obiri, PhD,
Nicole K Trudel,
Nikisha M Bolden,
Omotunde O Osunsanmi,
Pankaj H Amin,
Paul L Figarole, Jr,
Paula A Trost,
Peter E Baker,
Peter Kessler, PhD,
Prabhu P Raju,
Raymond T Oji,
Rebecca K Olin,
Rebecca Rodriguez,
Rebecca T Davis,
Richard W Thornton,
Riley C Myers, PhD,
Robert D Tollefsen,
Robert Jennings,
Robert Sausville,
Robin Levis, PhD,
Rose Ashley,
Sandra S Saniga,
Sarah B Tanksley,
Scott E Norris,
Scott N Lim,
Serge L Beaucage,
Sheilyn H Huang,
Shelley H Beausoleil,
Sherri J Jackson,
Sidney B Priesmeyer,
Solomon Yimam (SY),
Sonya M Edmonds,
Stephanie A Slater, MS,
Steven A Rubin,
Stuart W Russell,
Susan F Laska, MS,
Susan M Jackson,
Susan Yu,
Thai D Truong,
Thea C Grome,
Thuy T Nguyen, LCDR,
Tim Lee,
Timothy C Grome,
Tina S Roecklein,
Travis S Bradley,
Truong Xuan Nguyen (Andy),
Unnee Ranjan,
Walden H Lee,
Wanda Y Honeyblue,
Wei Wang, PhD,
William V Millar,
Yasamin Ameri,
Yi Wang, PhD,
Yiping Jia
Laurie P Norwood's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| March, 2003 | FDA 483 | Biopure Corporation - Form 483, 2003-03-27 |
| March, 2005 | FDA 483 | Sanofi Pasteur Inc. - Form 483, 2005-03-18 |
| May, 2014 | EIR | GSK Vaccines GmbH - EIR, 2014-05-06 |
| March, 2001 | FDA 483 Response | Seqirus Vaccines Limited - Form 483R, 2001-04-20 |
| March, 2001 | EIR | Seqirus Vaccines Limited - EIR, 2001-04-30 |
| March, 2001 | FDA 483 | Evans Vaccines Ltd. - Form 483, 2001-03-09 |
| January, 2000 | FDA 483 | Genentech, Inc. - Form 483, 2000-01-14 |
| May, 2014 | FDA 483 | GSK Vaccines GmbH - Form 483, 2014-05-06 |
| March, 2001 | FDA 483 Response | Seqirus Vaccines Limited - Form 483R, 2001-04-20 |
| October, 2003 | FDA 483 | Wyeth Farma SA - Form 483, 2003-10-29 |
| January, 2000 | EIR | Genentech, Inc. - EIR, 2000-01-14 |
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