FDA Investigator

Frank Wackes

Latest inspection on record: Saint Louis, United States, March 2017 · records back to 2015

Human DrugsMedical Devices & Rad Health

FDA inspection record · Last updated July 12, 2026

Overview

  • 7 inspections across 7 sites are on record.
  • 59 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2017-03-24.

At a glance

Inspections

7

Sites

7

Observations

59

Career since

Nov 2015

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Meridian Medical Technologies, LLC24 Mar 2017Medical Devices & Rad HealthView 483 →
Sigma-Aldrich Manufacturing LLC10 Mar 2017Human DrugsOn file
Nephron Sterile Compounding Center, LLC20 Jan 2017Human DrugsView 483 →
Kimball Electronics - Indianapolis1 Dec 2016Human Drugs
GP Grenzach Produktions GmbH1 Jul 2016Human DrugsView 483 →

Sites inspected

Meridian Medical Technologies, LLCSaint Louis, United States1 insp.
Sigma-Aldrich Manufacturing LLCSaint Louis, United States1 insp.
Nephron Sterile Compounding Center, LLCWest Columbia, United States1 insp.
Kimball Electronics - IndianapolisIndianapolis, United States1 insp.
GP Grenzach Produktions GmbHGrenzach-Wyhlen, Germany1 insp.

Co-investigators

Investigators who share inspections with this person.

Full investigator report

Get the verbatim findings behind Frank Wackes' 59 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