FDA-Inspected Site

Boehringer Ingelheim Pharmaceuticals, Inc.

8 FDA inspections are on record for Boehringer Ingelheim Pharmaceuticals, Inc. in Ridgefield, United States.

483· Form 483 issued

Ridgefield, United States · Last updated August 15, 2026

Overview

  • 8 FDA inspections are on record.
  • 4 inspections produced a Form 483.
  • The most recent recorded inspection date is 2018-12-06.

At a glance

Inspections

8

Form 483s

4

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
12 Nov 2018 – 6 Dec 2018Human Drugs483View 483 →
20 Jun 2018 – 3 Jul 2018Human Drugs483On file
21 Feb 2017 – 28 Feb 2017Human Drugs483View 483 →
14 Sep 2015 – 6 Oct 2015Human DrugsClean
28 Sep 2011Not recorded483On file
25 Sep 2009Not recordedClean
30 Sep 2005Not recordedClean
16 Jan 2001Not recordedClean

Observations on record

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

6 Dec 2018
21 CFR 312.50

General responsibilities of sponsors

Cited by Victoria M Daddeo

28 Feb 2017
21 CFR 312.50

General responsibilities of sponsors

Cited by Kent A Conforti

28 Feb 2017
21 CFR 312.50

General responsibilities of sponsors

Cited by Kent A Conforti

Investigators

FDA investigators tied to this site in the record.

Michelle M Noe Varga1 insp.
Mark R Mcclain1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 312.50Cited across public-safe Form 483 observations3x

Full site report

Get the verbatim findings behind Boehringer Ingelheim Pharmaceuticals, Inc.'s 4 Form 483s

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