FDA Documents of Dako North America Inc.
Dako North America Inc. is an organization that has been audited by the FDA 12 times between 2003 and 2019 across all 2 sites.
Documents
FDA 483 Dako North America, Carpinteria | October 2015
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Issued on: Oct 23, 2015
Medical Devices & Rad Health Form 483
FDA 483 Dako North America Inc., Carpinteria | 2017
Out-of-stock
Issued on: Oct 27, 2017
Medical Devices & Rad Health Form 483
FDA 483 Dako North America Inc., Carpinteria | 2017
Out-of-stock
Issued on: Jan 13, 2017
Medical Devices & Rad Health Form 483
FDA 483 Dako North America Inc., Carpinteria | 2012
Out-of-stock
Issued on: Oct 1, 2012
Medical Devices & Rad Health Form 483
FDA 483 Dako North America Inc., Carpinteria | 2008
Out-of-stock
Issued on: Mar 31, 2008
Medical Devices & Rad Health Form 483
FDA 483 Dako North America Inc., Carpinteria | 2005
Out-of-stock
Issued on: Oct 26, 2005
Medical Devices & Rad Health Form 483
FDA Investigators(10)
- Kelvin Cheung, FDA Investigator
- MDSAP WilliamsA, FDA Investigator
- Sonya L. Karsik, FDA Investigator
- Janet Pulver, FDA Investigator
- Leonard H. Lavi, FDA Investigator
- James R. Fleckenstein, FDA Investigator
- Sarah A. Hassas, FDA Investigator
- Scott K. Zika, FDA Investigator
- Francis J. Eng, FDA Investigator
- Allen F. Hall, FDA Investigator