FDA-Inspected Site

Acadia Pharmaceuticals, Inc

2 FDA inspections are on record for Acadia Pharmaceuticals, Inc in San Diego, United States.

483· Form 483 issued

San Diego, United States · Last updated July 10, 2026

Overview

  • 2 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2021-01-27.

At a glance

Inspections

2

Form 483s

2

EIRs

1

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
4 Jan 2021 – 27 Jan 2021Human Drugs483On file
19 Jan 2016 – 17 Feb 2016Human Drugs483View 483 →

Observations on record

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

17 Feb 2016
21 CFR 312.56(a)

Monitoring investigations

Cited by Lakecha N Lewis, Phillip D Kronstein, Ni A Khin

17 Feb 2016
21 CFR 312.50

General responsibilities of sponsors

Cited by Lakecha N Lewis, Phillip D Kronstein, Ni A Khin

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 312.50Cited across public-safe Form 483 observations1x
21 CFR 312.56(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Acadia Pharmaceuticals, 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