FDA Documents of Merck Serono Aubonne
Merck Serono Aubonne is an organization that has been audited by the FDA 9 times between 2000 and 2013 across all 1 sites.
Documents
FDA 483 Merck Serono Aubonne, Aubonne | 2013
Out-of-stock
Issued on: Nov 12, 2013
Human Drug Form 483
FDA 483 Merck Serono Aubonne, Aubonne | 2012
Out-of-stock
Issued on: Nov 16, 2012
Human Drug Form 483
FDA 483 Merck Serono Aubonne, Aubonne | 2011
Out-of-stock
Issued on: Jun 16, 2011
Human Drug Form 483
FDA 483 Merck Serono Aubonne, Aubonne | 2009
Out-of-stock
Issued on: Dec 9, 2009
Human Drug Form 483
FDA 483 Merck Serono Aubonne, Aubonne | 2007
Out-of-stock
Issued on: Jul 17, 2007
Human Drug Form 483
FDA 483 Merck Serono Aubonne, Aubonne | 2004
Out-of-stock
Issued on: Nov 19, 2004
Human Drug Form 483
FDA 483 Merck Serono Aubonne, Aubonne | 2000
Out-of-stock
Issued on: Jun 15, 2000
Human Drug Form 483
FDA Investigators(15)
- Michael E. Maselli, FDA Investigator
- Erika V. Butler, FDA Investigator
- Barbara J. Breithaupt, FDA Investigator
- Katherine Szestypalow, FDA Investigator
- Cynthia Jim, FDA Investigator
- Miguel A. Martinez, FDA Investigator
- Larry K. Austin, FDA Investigator
- Rose M. Ashley, FDA Investigator
- Julie D. Bringger, FDA Investigator
- Susan T. Hadman, FDA Investigator
- Melissa J. Garcia, FDA Investigator
- Gerald B. Seaborn, FDA Investigator
- Rochelle K. Kimmel, FDA Investigator
- Paul L. Figarole, FDA Investigator
- Ronald G. Crawford, FDA Investigator