FDA Documents of Agilent Technologies Inc
Agilent Technologies Inc is an organization that has been audited by the FDA 19 times between 2002 and 2023 across all 6 sites.
Documents
FDA 483 Agilent Technologies, Santa Clara | February 2017
Available Now - $199
Issued on: Feb 17, 2017
Medical Devices & Rad Health Form 483
FDA 483 Agilent Technologies, Santa Clara | July 2015
Available Now - $199
Issued on: Jul 6, 2015
Medical Devices & Rad Health Form 483
FDA 483 Agilent Technologies Inc, Boulder | 2019
Out-of-stock
Issued on: Aug 2, 2019
Human Drug Form 483
FDA 483 Agilent Technologies Inc, Lake Forest | 2006
Out-of-stock
Issued on: May 11, 2006
Medical Devices & Rad Health Form 483
FDA 483 Agilent Technologies Inc, Santa Rosa | 2004
Out-of-stock
Issued on: Aug 26, 2004
Medical Devices & Rad Health Form 483
FDA Investigators(16)
- Stephen C. Smith, FDA Investigator
- Rebecca T. Davis, FDA Investigator
- Erika V. Butler, FDA Investigator
- Zachary L. Stamm, FDA Investigator
- Zachary A. Bogorad, FDA Investigator
- Jamie L. Dion, FDA Investigator
- Quynh Strandberg, FDA Investigator
- Zachery L. Miller, FDA Investigator
- Mark E. Chan, FDA Investigator
- Cntrctmntr Anderson, FDA Investigator
- Kirtida Patel, FDA Investigator
- Francis J. Eng, FDA Investigator
- Trudy R. Papson, FDA Investigator
- Richard W. Tubb, FDA Investigator
- Charles I. Ahn, FDA Investigator
- John L. Stevens, FDA Investigator