FDA-Inspected Site

Regeneron Pharmaceuticals Inc

13 FDA inspections are on record for Regeneron Pharmaceuticals Inc in Tarrytown, United States.

Clean· No action indicated

Tarrytown, United States · Last updated July 10, 2026

Overview

  • 13 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-12-10.

At a glance

Inspections

13

Form 483s

1

EIRs

2

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
8 Dec 2025 – 10 Dec 2025Human DrugsClean
15 Apr 2024 – 1 May 2024Human DrugsClean
8 Jan 2024 – 19 Jan 2024Human DrugsClean
12 Oct 2021 – 15 Oct 2021Human DrugsClean
14 Dec 2020 – 21 Dec 2020Human DrugsClean
13 Jan 2020 – 17 Jan 2020Human DrugsClean
4 Sep 2018 – 17 Sep 2018Human DrugsClean
6 Aug 2018 – 10 Aug 2018Human DrugsClean
11 Jun 2018 – 18 Jun 2018Human DrugsClean
27 Jun 2017 – 30 Jun 2017Human DrugsClean
28 Nov 2016 – 30 Nov 2016Human DrugsClean
6 Feb 2013 – 22 Feb 2013Human Drugs483View 483 →

Observations on record

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

22 Feb 2013
21 CFR 600.80(b)

Review of Adverse Experiences - SOPs

Cited by Paul C Mouris

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 600.80(b)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Regeneron Pharmaceuticals Inc's 1 Form 483

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