FDA Documents of Gyrus ACMI, Inc.
Gyrus ACMI, Inc. is an organization that has been audited by the FDA 19 times between 2001 and 2023 across all 7 sites.
Documents
FDA 483 Gyrus ACMI, Inc., Littleton | 2023
Out-of-stock
Issued on: Nov 2, 2023
Medical Devices & Rad Health Form 483
FDA 483 Gyrus ACMI, Inc., Norwalk | 2017
Out-of-stock
Issued on: Dec 15, 2017
Medical Devices & Rad Health Form 483
FDA 483 Gyrus ACMI, Inc., Stamford | 2013
Out-of-stock
Issued on: May 31, 2013
Medical Devices & Rad Health Form 483
FDA 483 Gyrus ACMI, Inc., Stamford | 2012
Out-of-stock
Issued on: Aug 2, 2012
Medical Devices & Rad Health Form 483
FDA 483 Gyrus ACMI, Inc., Norwalk | 2011
Out-of-stock
Issued on: Oct 28, 2011
Medical Devices & Rad Health Form 483
FDA 483 Gyrus ACMI, Inc., Norwalk | 2004
Out-of-stock
Issued on: Jul 7, 2004
Medical Devices & Rad Health Form 483
FDA Investigators(19)
- Sunita Pandey, FDA Investigator
- Javelle P. Spann, FDA Investigator
- Benjamin W. Anderson, FDA Investigator
- Nicholas T. Domer, FDA Investigator
- Javonica F. Penn, FDA Investigator
- Mary A. Millner, FDA Investigator
- Susan M. Matthias, FDA Investigator
- Ralph W. Jerndal, FDA Investigator
- Rafael A. Kaup, FDA Investigator
- Jeffrey J. Thibodeau, FDA Investigator
- Michael G. Mayfield, FDA Investigator
- Rosanna M. Goodrich, FDA Investigator
- Dominic R. Frasca, FDA Investigator
- Laureen M. Geniusz, FDA Investigator
- Allison E. Sincek, FDA Investigator
- Mary E. Storch, FDA Investigator
- Benjamin J. Dastoli, FDA Investigator
- R.Terry Bolen, FDA Investigator
- Bolen, R.Terry, FDA Investigator