FDA Documents of Daito Pharmaceutical Co., Ltd.

Daito Pharmaceutical Co., Ltd. is an organization that has been audited by the FDA 9 times between 2006 and 2023 across all 3 sites.

Documents

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama | 2023

Out-of-stock
Issued on: Dec 19, 2023
Human Drugs Form 483

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama | 2022

Out-of-stock
Issued on: Sep 16, 2022
Human Drug Form 483

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama | 2020

Out-of-stock
Issued on: Jan 31, 2020
Human Drug Form 483

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama | 2017

Out-of-stock
Issued on: Nov 10, 2017
Human Drug Form 483

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama -City | 2013

Out-of-stock
Issued on: Oct 10, 2013
Human Drug Form 483

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama | 2013

Out-of-stock
Issued on: Oct 10, 2013
Human Drug Form 483

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama -City | 2011

Out-of-stock
Issued on: Sep 29, 2011
Human Drug Form 483

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama -City | 2008

Out-of-stock
Issued on: Feb 25, 2008
Human Drug Form 483

FDA 483 Daito Pharmaceutical Co., Ltd., Toyama -City | 2006

Out-of-stock
Issued on: Apr 20, 2006
Human Drug Form 483