FDA Documents of Kyowa Hakko Bio Co., Ltd.
Kyowa Hakko Bio Co., Ltd. is an organization that has been audited by the FDA 11 times between 2007 and 2022 across all 5 sites.
Documents
FDA 483 Kyowa Hakko Bio Co., Ltd., Hofu | 2022
Out-of-stock
Issued on: Apr 15, 2022
Human Drug Form 483
FDA 483 Kyowa Hakko Bio Co., Ltd., Hofu | 2019
Out-of-stock
Issued on: Nov 8, 2019
Human Drug Form 483
FDA 483 Kyowa Hakko Bio Co., Ltd., Ube | 2017
Out-of-stock
Issued on: Sep 15, 2017
Human Drug Form 483
FDA 483 Kyowa Hakko Bio Co., Ltd., Hofu | 2017
Out-of-stock
Issued on: Sep 8, 2017
Human Drug Form 483
FDA 483 Kyowa Hakko Bio Co., Ltd., Ube City | 2014
Out-of-stock
Issued on: Mar 14, 2014
Human Drug Form 483
FDA 483 Kyowa Hakko Bio Co., Ltd., Hofu City | 2011
Out-of-stock
Issued on: Oct 27, 2011
Human Drug Form 483
FDA 483 Kyowa Hakko Bio Co., Ltd., Hofu City | 2010
Out-of-stock
Issued on: Jun 25, 2010
Human Drug Form 483
FDA 483 Kyowa Hakko Bio Co., Ltd., Hofu City | 2007
Out-of-stock
Issued on: Aug 23, 2007
Human Drug Form 483
FDA Investigators(10)
- Teresa I. Navas, FDA Investigator
- Margaret M. Annes, FDA Investigator
- Sneha S. Patel, FDA Investigator
- Marcus F. Yambot, FDA Investigator
- Milva E. Melendez, FDA Investigator
- Angela E. Glenn, FDA Investigator
- Douglas C. Kovacs, FDA Investigator
- Yumi J. Hiramine, FDA Investigator
- Luis A. Dasta, FDA Investigator
- Rochelle B. Young, FDA Investigator