FDA Documents of FujiFilm Diosynth Biotechnologies U.S.A., Inc.
FujiFilm Diosynth Biotechnologies U.S.A., Inc. is an organization that has been audited by the FDA 8 times between 2015 and 2023 across all 1 sites.
Documents
FDA 483 FujiFilm Diosynth Biotechnologies U | May 2015
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Issued on: May 1, 2015
Human Drug Form 483
FDA 483 FujiFilm Diosynth Biotechnologies U.S.A., Inc., Research Triangle Park | 2023
Out-of-stock
Issued on: Feb 10, 2023
Human Drugs Form 483
FDA 483 FujiFilm Diosynth Biotechnologies U.S.A., Inc., Research Triangle Park | 2021
Out-of-stock
Issued on: Apr 21, 2021
Human Drug Form 483
FDA 483 FujiFilm Diosynth Biotechnologies U.S.A., Inc., Research Triangle Park | 2019
Out-of-stock
Issued on: Mar 1, 2019
Human Drug Form 483
FDA 483 FujiFilm Diosynth Biotechnologies U.S.A., Inc., Research Triangle Park | 2019
Out-of-stock
Issued on: Feb 22, 2019
Human Drug Form 483
FDA 483 FujiFilm Diosynth Biotechnologies U.S.A., Inc., Research Triangle Park | 2018
Out-of-stock
Issued on: Oct 26, 2018
Human Drug Form 483
FDA Investigators(15)
- Yuan-Chia Kuo, FDA Investigator
- Jee Y. Chung, FDA Investigator
- Charles Y. Kuo,
- Seneca D. Toms, FDA Investigator
- Jacek Cieslak, FDA Investigator
- Yun Wu, FDA Investigator
- Zhihao Pete Qiu, FDA Investigator
- Veronica Fuentes, FDA Investigator
- Thuy T. Nguyen, FDA Investigator
- Amy A. Devlin, FDA Investigator
- Steven Fong, FDA Investigator
- V Ashutosh Rao, FDA Investigator
- Sonya M. Edmonds, FDA Investigator
- Bonita S. Chester, FDA Investigator
- Bo Chi, FDA Investigator