FDA Documents of Navajo Manufacturing Company, Inc
Navajo Manufacturing Company, Inc is an organization that has been audited by the FDA 10 times between 2002 and 2018 across all 2 sites.
Documents
FDA 483 Navajo Manufacturing Company, Inc, Denver | 2013
Out-of-stock
Issued on: Jul 9, 2013
Human Drug Form 483
FDA 483 Navajo Manufacturing Company, Inc, Denver | 2012
Out-of-stock
Issued on: Jun 11, 2012
Human Drug Form 483
FDA 483 Navajo Manufacturing Company, Inc, Denver | 2011
Out-of-stock
Issued on: Jan 28, 2011
Human Drug Form 483
FDA 483 Navajo Manufacturing Company, Inc, Denver | 2010
Out-of-stock
Issued on: Mar 11, 2010
Medical Devices & Rad Health Form 483
FDA 483 Navajo Manufacturing Company, Inc, Denver | 2009
Out-of-stock
Issued on: Dec 29, 2009
Human Drug Form 483
FDA 483 Navajo Manufacturing Company, Inc, Denver | 2003
Out-of-stock
Issued on: Apr 30, 2003
Human Drug Form 483
FDA 483 Navajo Manufacturing Company, Inc, Denver | 2002
Out-of-stock
Issued on: Jul 10, 2002
Human Drug Form 483
FDA Investigators(9)
- Jamie L. Dion, FDA Investigator
- Christine I. Shaw, FDA Investigator
- Edith M. Gonzalez, FDA Investigator
- Isabel Y. Espinosa, FDA Investigator
- Caroline H. Le, FDA Investigator
- Linda M. Cherry, FDA Investigator
- Debra L. Curtis, FDA Investigator
- Matthew R. Dionne, FDA Investigator
- Patricia A. Brown, FDA Investigator