FDA Investigator

Michael F Skelly

Latest inspection on record: Tarrytown, United States, January 2020 · records back to 2016

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 9 inspections across 9 sites are on record.
  • 2 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2020-01-17.

At a glance

Inspections

9

Sites

9

Observations

2

Career since

Jan 2016

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Regeneron Pharmaceuticals Inc17 Jan 2020Human Drugs
Celerion Inc11 Jan 2019Human Drugs
BioAgilytix Labs LLC27 Jul 2018Human Drugs
QPS, LLC8 Dec 2017Human Drugs
Pra Health Sciences12 May 2017Human Drugs

Sites inspected

Regeneron Pharmaceuticals IncTarrytown, United States1 insp.
Celerion IncLincoln, United States1 insp.
BioAgilytix Labs LLCDurham, United States1 insp.
QPS, LLCNewark, United States1 insp.
Pra Health SciencesAssen, Netherlands1 insp.

Co-investigators

Investigators who share inspections with this person.

Full investigator report

Get the verbatim findings behind Michael F Skelly's 2 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