Shire Human Genetic Therapies Inc
FDA-inspected organization
Shire Human Genetic Therapies Inc has been audited by the FDA 48 times between 2008 and 2022 across all 7 sites.
Documents
FDA 483 Shire Human Genetic Therapies Inc, Lexington | 2022
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Lexington | 2015
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, North Reading | 2014
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Cambridge | 2013
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Lexington | 2013
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Lexington | 2013
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Lexington | 2012
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Lexington | 2012
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, North Reading | 2012
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Cambridge | 2011
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Lexington | 2009
Out of stock
FDA 483 Shire Human Genetic Therapies Inc, Cambridge | 2009
Out of stock
FDA Investigators (19)
- Robert J. Martin, FDA Investigator
- Wayne E. Seifert, FDA Investigator
- Scott C. Lute, FDA Investigator
- Rachael O. Oyewole, FDA Investigator
- Edmund F. Mrak, FDA Investigator
- MDSAP harperd, FDA Investigator
- Sean R. Marcsisin, FDA Investigator
- Deborah J. Parris, FDA Investigator
- Mary-Jeanet McGarry, FDA Investigator
- Debra M. Emerson, FDA Investigator
- Thomas J. Arista, FDA Investigator
- Megan A. Haggerty, FDA Investigator
- Ellen P. Madigan, FDA Investigator
- Ramon E. Martinez, FDA Investigator
- Michelle M. Noe, FDA Investigator
- Rory Geyer, FDA Investigator
- Kalavati C. Suvarna, FDA Investigator
- Robert C. Horan, FDA Investigator
- Richard H. Penta, FDA Investigator