FDA-Inspected Site

Acclarent, Inc.

4 FDA inspections are on record for Acclarent, Inc. in Irvine, United States.

Clean· No action indicated

Irvine, United States · Last updated July 10, 2026

Overview

  • 4 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2020-09-25.

At a glance

Inspections

4

Form 483s

2

EIRs

1

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
22 Sep 2020 – 25 Sep 2020Medical Devices & Rad HealthClean
31 Oct 2013 – 9 Dec 2013Medical Devices & Rad HealthClean
29 Jan 2013 – 22 Feb 2013Medical Devices & Rad HealthWLView 483 →
24 Feb 2012Not recordedWLOn file

Observations on record

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

22 Feb 2013
21 CFR 806.10(a)(1)

Report of risk to health

Cited by Lydia S Chan

22 Feb 2013
21 CFR 820.30(g)

Design validation- Lack of or inadequate procedures

Cited by Lydia S Chan

Investigators

FDA investigators tied to this site in the record.

Alla Dubrovsky1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 806.10(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Acclarent, Inc.'s 2 Form 483s

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