FDA-Inspected Site

Catalent Micron Technologies, Inc.

6 FDA inspections are on record for Catalent Micron Technologies, Inc. in Malvern, United States.

483· Form 483 issued

Malvern, United States · Last updated July 10, 2026

Overview

  • 6 FDA inspections are on record.
  • 3 inspections produced a Form 483.
  • The most recent recorded inspection date is 2025-06-09.

At a glance

Inspections

6

Form 483s

3

EIRs

1

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
2 Jun 2025 – 9 Jun 2025Human Drugs483On file
18 Mar 2019 – 21 Mar 2019Human DrugsClean
14 Apr 2016 – 20 Apr 2016Human Drugs483On file
11 Jun 2013 – 12 Jun 2013Human DrugsClean
8 Dec 2010Not recorded483View 483 →
23 Feb 2010Not recordedClean

Observations on record

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

8 Dec 2010
21 CFR 211.160(a)

Lab controls established, including changes

Cited by Vlada Matusovsky

8 Dec 2010
21 CFR 211.192

Written record of investigation incomplete

Cited by Vlada Matusovsky

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 211.160(a)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Catalent Micron Technologies, Inc.'s 3 Form 483s

Source PDFs, 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