FDA-Inspected Site

Global Product Management, Inc.

2 FDA inspections are on record for Global Product Management, Inc. in Monrovia, United States.

483· Form 483 issued

Monrovia, 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 2018-04-18.

At a glance

Inspections

2

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
20 Mar 2018 – 18 Apr 2018Foods & Cosmetics483View 483 →
7 Mar 2011Not recorded483View 483 →

Observations on record

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

18 Apr 2018
21 CFR 111.73

Specifications met - received product identified

Cited by Kevin Lee

7 Mar 2011
21 CFR 111.103

Written procedures - quality control operations

Cited by Marcus F Yambot, Julia Ventura

7 Mar 2011
21 CFR 111.105(i)

QC required operations production and process control

Cited by Marcus F Yambot, Julia Ventura

7 Mar 2011
21 CFR 111.105(i)

Quality control - required operations product complaints

Cited by Marcus F Yambot, Julia Ventura

7 Mar 2011
21 CFR 111.315(b)(5)

Sampling plans; packaged, labeled dietary supplement, QC

Cited by Marcus F Yambot, Julia Ventura

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 111.105(i)Cited across public-safe Form 483 observations2x
21 CFR 111.103Cited across public-safe Form 483 observations1x
21 CFR 111.315(b)(5)Cited across public-safe Form 483 observations1x
21 CFR 111.570(b)(1)Cited across public-safe Form 483 observations1x
21 CFR 111.73Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Global Product Management, 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