FDA Documents of Fresenius Kabi USA, LLC

Fresenius Kabi USA, LLC is an organization that has been audited by the FDA 77 times between 2000 and 2024 across all 7 sites.

Documents

FDA 483 Fresenius Kabi USA, LLC, Grand Island | 2023

Out-of-stock
Issued on: Aug 30, 2023
Medical Devices & Rad Health Form 483

FDA 483 Fresenius Kabi USA, LLC, Grand Island | 2019

Out-of-stock
Issued on: Aug 12, 2019
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Grand Island | 2018

Out-of-stock
Issued on: Jun 29, 2018
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Grand Island | 2017

Out-of-stock
Issued on: Mar 30, 2017
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Wilson | 2016

Out-of-stock
Issued on: Jun 24, 2016
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Grand Island | 2016

Out-of-stock
Issued on: Feb 4, 2016
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Melrose Park | 2015

Out-of-stock
Issued on: Sep 1, 2015
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Grand Island | 2014

Out-of-stock
Issued on: Oct 24, 2014
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Melrose Park | 2013

Out-of-stock
Issued on: Dec 11, 2013
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Grand Island | 2013

Out-of-stock
Issued on: Jan 11, 2013
Human Drug Form 483

FDA 483 Fresenius Kabi USA, LLC, Lake Zurich | 2012

Out-of-stock
Issued on: May 4, 2012
Human Drug Form 483

FDA Investigators(70)