FDA Documents of Taro Pharmaceutical Industries, Ltd.
Taro Pharmaceutical Industries, Ltd. is an organization that has been audited by the FDA 9 times between 2002 and 2022 across all 4 sites.
Documents
FDA 483 Taro Pharmaceutical, Haifa | July 2019
Available Now - $199
Issued on: Jul 11, 2019
Human Drug Form 483
FDA 483 Taro Pharmaceutical Industries, Ltd., Haifa | 2017
Out-of-stock
Issued on: Feb 5, 2017
Human Drug Form 483
FDA 483 Taro Pharmaceutical Industries, Ltd., Haifa | 2015
Out-of-stock
Issued on: May 21, 2015
Human Drug Form 483
FDA 483 Taro Pharmaceutical Industries, Ltd., Haifa Bay | 2010
Out-of-stock
Issued on: May 28, 2010
Human Drug Form 483
FDA 483 Taro Pharmaceutical Industries, Ltd., Haifa Bay | 2009
Out-of-stock
Issued on: Sep 10, 2009
Human Drug Form 483
FDA 483 Taro Pharmaceutical Industries, Ltd., Haifa Bay | 2002
Out-of-stock
Issued on: Oct 31, 2002
Human Drug Form 483
FDA Investigators(19)
- Norman K. Starks, FDA Investigator
- Michael Araneta, FDA Investigator
- Yvesna C. Blaise, FDA Investigator
- Walden H. Lee, FDA Investigator
- Zhongren Wu, FDA Investigator
- Pratik S. Upadhyay, FDA Investigator
- Leonard H. Lavi, FDA Investigator
- Sandra A. Hughes, FDA Investigator
- Concepcion Cruz, FDA Investigator
- Derek Smith, FDA Investigator
- Simone E. Pitts, FDA Investigator
- Jose A. Lopez Rubet, FDA Investigator
- Lopez Rubet, Jose A, FDA Investigator
- Margaret M. Annes, FDA Investigator
- Cynthia J. Lee, FDA Investigator
- Katherine E. Jacobitz, FDA Investigator
- Wayne T. Smith, FDA Investigator
- Thomas J. Arista, FDA Investigator
- Robert D. Tollefsen, FDA Investigator