FDA Investigator

Paul C Mouris

Latest inspection on record: Burlington, United States, May 2023 · records back to 2008

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 69 inspections across 54 sites are on record.
  • 140 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2023-05-12.

At a glance

Inspections

69

Sites

54

Observations

140

Career since

Feb 2008

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Quality Packaging Specialists International, LLC12 May 2023Human Drugs
CHARLES RIVER LABORATORIES19 Mar 2020Human Drugs
Greenbrier International, Inc18 Jan 2019Human DrugsOn file
Cipla Limited13 Apr 2018Human DrugsOn file
Chartwell Pharmaceuticals Carmel, LLC.23 Dec 2013Human DrugsView 483 →

Sites inspected

Quality Packaging Specialists International, LLCBurlington, United States1 insp.
CHARLES RIVER LABORATORIESWayne, United States1 insp.
Greenbrier International, IncChesapeake, United States1 insp.
Cipla LimitedPithampur, District Dhar, India1 insp.
Chartwell Pharmaceuticals Carmel, LLC.Carmel, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Sony Mathews3 shared
James D Bridges2 shared
Gary J Lehr2 shared

Full investigator report

Get the verbatim findings behind Paul C Mouris' 140 observations

Source 483 PDFs, verbatim observations, and how each site responded, so your team knows what they cite before they arrive.

  • New inspections and Form 483s, mapped to the CFR citation
  • Warning letter outcomes, and the citation patterns they repeat
  • Their co-investigators, so no surprises about who shows up on site