FDA-Inspected Site

API, Inc.

9 FDA inspections are on record for API, Inc. in Fairfield, United States.

483· Form 483 issued

Fairfield, United States · Last updated July 10, 2026

Overview

  • 9 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2024-08-08.

At a glance

Inspections

9

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
1 Aug 2024 – 8 Aug 2024Human Drugs483On file
23 Jan 2017 – 26 Jan 2017Human DrugsClean
11 Mar 2014 – 13 Mar 2014Human DrugsClean
6 Apr 2012Not recordedClean
15 Jul 2011Not recorded483On file
28 Mar 2007Not recordedClean
25 Mar 2005Not recordedClean
30 Jan 2004Not recordedClean
21 Aug 2001Not recordedClean

Investigators

FDA investigators tied to this site in the record.

Full site report

Get the verbatim findings behind API, Inc.'s 2 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