FDA Investigator

Diane M Biron

Latest inspection on record: Merrimack, United States, November 2024 · records back to 2016

Medical Devices & Rad Health

FDA inspection record · Last updated July 12, 2026

Overview

  • 12 inspections across 9 sites are on record.
  • 104 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2024-11-26.

At a glance

Inspections

12

Sites

9

Observations

104

Career since

Feb 2016

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Atrium Medical Corporation26 Nov 2024Medical Devices & Rad HealthView 483 →
Integra LifeSciences Corporation5 Jun 2024Medical Devices & Rad HealthView 483 →
Professional Contract Sterilization, Inc.16 Feb 2024Medical Devices & Rad HealthView 483 →
TEI Biosciences, Inc.17 May 2023Medical Devices & Rad HealthView 483 →
LeMaitre Vascular, Inc.15 Jun 2022Medical Devices & Rad HealthView 483 →

Sites inspected

Atrium Medical CorporationMerrimack, United States1 insp.
Integra LifeSciences CorporationMansfield, United States1 insp.
Professional Contract Sterilization, Inc.Taunton, United States1 insp.
TEI Biosciences, Inc.Boston, United States1 insp.
LeMaitre Vascular, Inc.Burlington, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Full investigator report

Get the verbatim findings behind Diane M Biron's 104 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