FDA Investigator

Lequita M Mayhew

Latest inspection on record: Itasca, United States, June 2019 · records back to 2008

Human DrugsMedical Devices & Rad HealthBiologics

FDA inspection record · Last updated July 12, 2026

Overview

  • 101 inspections across 96 sites are on record.
  • 133 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2019-06-19.

At a glance

Inspections

101

Sites

96

Observations

133

Career since

Mar 2008

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Topco Associates LLC19 Jun 2019Human Drugs
Danny H. Sugimoto, M.D.23 May 2019Human Drugs
Vifor Pharma Ltd29 Mar 2019Human DrugsView 483 →
Marianne Brodmann, MD22 Mar 2019Medical Devices & Rad HealthView 483 →
Akorn, Inc.5 Mar 2019Human Drugs

Sites inspected

Topco Associates LLCItasca, United States1 insp.
Danny H. Sugimoto, M.D.Chicago, United States1 insp.
Vifor Pharma LtdGlattbrugg, Switzerland1 insp.
Marianne Brodmann, MDGraz, Austria1 insp.
Akorn, Inc.Lake Forest, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Debra L Boyd Seale3 shared
Debra I Love2 shared

Full investigator report

Get the verbatim findings behind Lequita M Mayhew's 133 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