FDA Documents of Vitrolife, Inc.
Vitrolife, Inc. is an organization that has been audited by the FDA 12 times between 2003 and 2021 across all 4 sites.
Documents
FDA 483 Vitrolife, San Diego | August 2021
Available Now - $199
Issued on: Aug 19, 2021
Medical Devices & Rad Health Form 483
FDA 483 Vitrolife, Englewood | February 2019
Available Now - $199
Issued on: Feb 13, 2019
Medical Devices & Rad Health Form 483
FDA 483 Vitrolife, Inc., San Diego | 2018
Out-of-stock
Issued on: Sep 21, 2018
Medical Devices & Rad Health Form 483
FDA 483 Vitrolife, Inc., Englewood | 2010
Out-of-stock
Issued on: Apr 16, 2010
Medical Devices & Rad Health Form 483
FDA 483 Vitrolife, Inc., San Diego | 2008
Out-of-stock
Issued on: Jan 31, 2008
Medical Devices & Rad Health Form 483
FDA 483 Vitrolife, Inc., San Diego | 2006
Out-of-stock
Issued on: Apr 13, 2006
Medical Devices & Rad Health Form 483
FDA 483 Vitrolife, Inc., San Diego | 2003
Out-of-stock
Issued on: Dec 22, 2003
Medical Devices & Rad Health Form 483
FDA Investigators(10)
- Angelica G. Aziz, FDA Investigator
- Christine I. Shaw, FDA Investigator
- Dianiris C. Ayala, FDA Investigator
- Marc A. Jackson, FDA Investigator
- Charles L. Larson, FDA Investigator
- Cntrctmntr Anderson, FDA Investigator
- Bryan J. Love, FDA Investigator
- Yvette E. Guillermo, FDA Investigator
- Kimetha A. King, FDA Investigator
- Scott K. Zika, FDA Investigator