Covance Laboratories Inc.August 17, 2018

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

View on Dashboard

Discuss this record with AI

ChatGPT

Claude

Perplexity

Grok

Copilot

Document or profile

One record shows the event. A profile shows the pattern.

Buy this document for the source file and details behind this single event.

Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.

Explore Covance Laboratories Inc.

Record Details

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.

Company: Covance Laboratories Inc.
Inspection Date: August 17, 2018
Product Type: Other
Office: Minneapolis District Office
People: Zhou Chen (issuing_officer)
Corey K. Reno (investigator)

Open in Dashboard

ID · 8e04cb00-5afa-410d-acb9-d17209fed7e7