FDA 483 - Covance Laboratories Inc. - August 17, 2018

This FDA Form 483 was issued to Covance Laboratories Inc. in Madison, WI, following a GLP - BIMO inspection. The inspection revealed two significant observations related to inadequate equipment validation and maintenance for tissue processors, and deficiencies in storage areas for animal feed and bedding, including failure to follow vendor assessment procedures. These issues indicate potential non-compliance with good laboratory practices.