FDA Investigator

Nicole E Knowlton

Latest inspection on record: Clearwater, United States, February 2026 · records back to 2009

Human DrugsAnimal Drugs & FeedsMedical Devices & Rad HealthFoods & Cosmetics

FDA inspection record · Last updated July 12, 2026

Overview

  • 239 inspections across 220 sites are on record.
  • 595 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-02-26.

At a glance

Inspections

239

Sites

220

Observations

595

Career since

Oct 2009

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
CoreRX Inc.26 Feb 2026Human DrugsOn file
Catalent Pharma Solutions, LLC30 Jan 2026Human DrugsOn file
International Contract Labs24 Nov 2025Human DrugsOn file
Catalent Greenville Inc24 Oct 2025Human DrugsView 483 →
Patheon Manufacturing Services LLC26 Sep 2025Human DrugsOn file

Sites inspected

CoreRX Inc.Clearwater, United States1 insp.
Catalent Pharma Solutions, LLCSaint Petersburg, United States1 insp.
International Contract LabsSt Petersburg, United States1 insp.
Catalent Greenville IncGreenville, United States1 insp.
Patheon Manufacturing Services LLCGreenville, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Jennifer A Robinson33 shared
Melanie G Warzala18 shared
Gene R Gunn10 shared
Cheryl A Clausen6 shared
Rozelle G Smith5 shared

Full investigator report

Get the verbatim findings behind Nicole E Knowlton's 595 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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