FDA Investigator

Melanie M Walker

Latest inspection on record: Greenville, United States, May 2024 · records back to 2008

Human DrugsMedical Devices & Rad Health

FDA inspection record · Last updated July 12, 2026

Overview

  • 21 inspections across 18 sites are on record.
  • 78 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2024-05-24.

At a glance

Inspections

21

Sites

18

Observations

78

Career since

Mar 2008

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Patheon Manufacturing Services LLC24 May 2024Human DrugsView 483 →
Gilead Sciences, Inc.12 Feb 2024Human DrugsView 483 →
Nephron Sterile Compounding Center, LLC10 Feb 2023Human DrugsView 483 →
King Bio Inc20 Jul 2018Human DrugsOn file
Nephron Pharmaceuticals Corp.14 Aug 2015Human DrugsOn file

Sites inspected

Patheon Manufacturing Services LLCGreenville, United States1 insp.
Gilead Sciences, Inc.La Verne, United States1 insp.
Nephron Sterile Compounding Center, LLCWest Columbia, United States1 insp.
King Bio IncAsheville, United States1 insp.
Nephron Pharmaceuticals Corp.Orlando, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Full investigator report

Get the verbatim findings behind Melanie M Walker's 78 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