FDA Investigator

Kathleen R Jones

Latest inspection on record: Stevenage, United Kingdom, April 2024 · records back to 2017

BiologicsHuman Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 16 inspections across 15 sites are on record.
  • 0 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2024-04-30.

At a glance

Inspections

16

Sites

15

Observations

0

Career since

May 2017

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
AUTOLUS LIMITED30 Apr 2024BiologicsOn file
Novartis Pharma Stein AG20 Nov 2023Biologics
GenIbet Biopharmaceuticals31 Jan 2023BiologicsOn file
Seres Therapeutics Inc14 Dec 2022Biologics
Aimmune Therapeutics Manufacturing, LLC9 Dec 2022Biologics

Sites inspected

AUTOLUS LIMITEDStevenage, United Kingdom1 insp.
Novartis Pharma Stein AGStein Ag, Switzerland1 insp.
GenIbet BiopharmaceuticalsOeiras, Portugal1 insp.
Seres Therapeutics IncCambridge, United States1 insp.
Aimmune Therapeutics Manufacturing, LLCWaltham, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Full investigator report

Get the verbatim findings behind Kathleen R Jones' inspection record

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