FDA Documents of KVK-Tech, Inc.

KVK-Tech, Inc. is an organization that has been audited by the FDA 20 times between 2006 and 2022 across all 2 sites.

Documents

FDA 483 KVK-Tech, Inc., Newtown | 2019

Out-of-stock
Issued on: Apr 16, 2019
Human Drug Form 483

FDA 483 KVK-Tech, Inc., Newtown | 2018

Out-of-stock
Issued on: Jan 24, 2018
Human Drug Form 483

FDA 483 KVK-Tech, Inc., Newtown | 2017

Out-of-stock
Issued on: Jun 27, 2017
Human Drug Form 483

FDA 483 KVK-Tech, Inc., Newtown | 2016

Out-of-stock
Issued on: Mar 14, 2016
Human Drug Form 483

FDA 483 KVK-Tech, Inc., Newtown | 2013

Out-of-stock
Issued on: Dec 9, 2013
Human Drug Form 483

FDA 483 KVK-Tech, Inc., Newtown | 2011

Out-of-stock
Issued on: Aug 1, 2011
Human Drug Form 483

FDA 483 KVK-Tech, Inc., Newtown | 2009

Out-of-stock
Issued on: Dec 16, 2009
Human Drug Form 483

FDA 483 KVK-Tech, Inc., Newtown | 2009

Out-of-stock
Issued on: Aug 31, 2009
Human Drug Form 483