FDA-Inspected Site

Bristol-Myers Squibb Company

9 FDA inspections are on record for Bristol-Myers Squibb Company in Devens, United States.

483· Form 483 issued

Devens, United States · Last updated July 9, 2026

Overview

  • 9 FDA inspections are on record.
  • 5 inspections produced a Form 483.
  • The most recent recorded inspection date is 2025-07-08.

At a glance

Inspections

9

Form 483s

5

EIRs

1

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
16 Jun 2025 – 8 Jul 2025Human Drugs483On file
1 May 2023 – 5 May 2023Biologics483On file
13 Oct 2021 – 20 Oct 2021Human DrugsClean
2 Jan 2020 – 10 Jan 2020Human Drugs483On file
16 Mar 2017 – 5 Apr 2017Human Drugs483On file
17 Oct 2016 – 21 Oct 2016Human DrugsClean
22 Jun 2015 – 26 Jun 2015Human DrugsClean
29 May 2013 – 20 Jun 2013Human Drugs483On file
13 Apr 2012Not recordedClean

Investigators

FDA investigators tied to this site in the record.

Lori M Newman1 insp.
Paul L Bellamy1 insp.
Megan A Haggerty1 insp.

Full site report

Get the verbatim findings behind Bristol-Myers Squibb Company's 5 Form 483s

The full inspection record, as Atlas holds it, 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