FDA Investigator

Meredith L Miller

Latest inspection on record: Springfield, United States, June 2026 · records back to 2023

Human DrugsMedical Devices & Rad HealthBiologicsFoods & Cosmetics

FDA inspection record · Last updated July 12, 2026

Overview

  • 49 inspections across 49 sites are on record.
  • 18 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-06-15.

At a glance

Inspections

49

Sites

49

Observations

18

Career since

Oct 2023

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Claudia T. Martorell, M.D.15 Jun 2026Human DrugsOn file
Michael S. Chapman, M.D.15 May 2026Human Drugs
Cogent Biosciences, Inc.24 Apr 2026Human Drugs
Erica L. Mayer, M.D.27 Mar 2026Human DrugsOn file
Parexel International (MA) Corporation5 Mar 2026Human Drugs

Sites inspected

Claudia T. Martorell, M.D.Springfield, United States1 insp.
Michael S. Chapman, M.D.Lebanon, United States1 insp.
Cogent Biosciences, Inc.Waltham, United States1 insp.
Erica L. Mayer, M.D.Boston, United States1 insp.
Parexel International (MA) CorporationAuburndale, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Agata E Libera1 shared

Full investigator report

Get the verbatim findings behind Meredith L Miller's 18 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

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