FDA Documents of Regis Technologies, Inc.
Regis Technologies, Inc. is an organization that has been audited by the FDA 11 times between 2000 and 2022 across all 1 sites.
Documents
FDA 483 Regis Technologies, Morton Grove | November 2022
Available Now - $199
Issued on: Nov 16, 2022
Human Drugs Form 483
FDA 483 Regis Technologies, Inc., Morton Grove | 2011
Out-of-stock
Issued on: Mar 8, 2011
Human Drug Form 483
FDA 483 Regis Technologies, Inc., Morton Grove | 2009
Out-of-stock
Issued on: May 8, 2009
Human Drug Form 483
FDA 483 Regis Technologies, Inc., Morton Grove | 2006
Out-of-stock
Issued on: May 3, 2006
Animal Drugs & Feed Form 483
FDA 483 Regis Technologies, Inc., Morton Grove | 2004
Out-of-stock
Issued on: Mar 5, 2004
Animal Drugs & Feed Form 483
FDA 483 Regis Technologies, Inc., Morton Grove | 2002
Out-of-stock
Issued on: Oct 15, 2002
Animal Drugs & Feed Form 483
FDA 483 Regis Technologies, Inc., Morton Grove | 2000
Out-of-stock
Issued on: Oct 5, 2000
Human Drug Form 483
FDA Investigators(14)
- Nibin Varghese, FDA Investigator
- Enrico-Jose T. Mangahis, FDA Investigator
- Nicholas P. Diorio, FDA Investigator
- Christopher D. Leach, FDA Investigator
- Brian D. Nicholson, FDA Investigator
- Christina A. Miller, FDA Investigator
- Denarvis C. Mendenhall, FDA Investigator
- Jason F. Chancey, FDA Investigator
- Lequita M. Mayhew, FDA Investigator
- Karen E. Masley-Joseph, FDA Investigator
- Carrie-Ann Plucinski, FDA Investigator
- Susan P. Bruederle, FDA Investigator
- Bruce H. McCullough, FDA Investigator
- Nicholas F. Lyons, FDA Investigator