FDA-Inspected Site

Covance, Inc.

8 FDA inspections are on record for Covance, Inc. in Dallas, United States.

Clean· No action indicated

Dallas, United States · Last updated July 9, 2026

Overview

  • 8 FDA inspections are on record.
  • 3 inspections produced a Form 483.
  • The most recent recorded inspection date is 2022-11-18.

At a glance

Inspections

8

Form 483s

3

EIRs

1

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
15 Nov 2022 – 18 Nov 2022Human DrugsClean
3 Jun 2019 – 7 Jun 2019Human Drugs483View 483 →
22 Feb 2017 – 28 Feb 2017Human DrugsClean
11 Jan 2016 – 20 Jan 2016Human DrugsClean
25 Jun 2013 – 2 Jul 2013Human Drugs483On file
21 Apr 2011Not recordedClean
3 Mar 2011Not recordedClean
1 Apr 2010Not recorded483On file

Observations on record

Form 483 observations cited at this site, most recent first.

7 Jun 2019
21 CFR 312.57(c)

Record retention requirement

Cited by Andrace Deyampert, Travis M Beard

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 312.57(c)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Covance, Inc.'s 3 Form 483s

Source PDFs, verbatim observations, and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat