FDA Investigator

Mark E Parmon

Latest inspection on record: Waltham, United States, September 2014 · records back to 2008

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 17 inspections across 17 sites are on record.
  • 8 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2014-09-22.

At a glance

Inspections

17

Sites

17

Observations

8

Career since

Mar 2008

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Genzyme A Sanofi Company22 Sep 2014Human Drugs
Genzyme Corporation18 Sep 2014Human Drugs
Masters Pharmaceuticals Inc.11 Aug 2014Human Drugs
Ferring Controlled Therapeutics Ltd.13 Dec 2012
Butterworth Laboratories Ltd5 Dec 2012

Sites inspected

Genzyme A Sanofi CompanyWaltham, United States1 insp.
Genzyme CorporationNorthborough, United States1 insp.
Masters Pharmaceuticals Inc.Fairfield, United States1 insp.
Ferring Controlled Therapeutics Ltd.Glasgow, United Kingdom1 insp.
Butterworth Laboratories LtdTeddington, United Kingdom1 insp.

Co-investigators

Investigators who share inspections with this person.

Tracey L Harris1 shared

Full investigator report

Get the verbatim findings behind Mark E Parmon's 8 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