FDA Investigator

Erika E Englund

Latest inspection on record: Tosu, Japan, December 2017 · records back to 2014

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 5 inspections across 4 sites are on record.
  • 20 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2017-12-08.

At a glance

Inspections

5

Sites

4

Observations

20

Career since

Mar 2014

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Oishi Koseido Co., Ltd.8 Dec 2017Human Drugs
Oishi Koseido Co., Ltd.6 Dec 2017Human Drugs
Fresenius Kabi USA, LLC30 Mar 2017Human DrugsOn file
Oishi Koseido Co., Ltd.29 Jan 2016Human DrugsView 483 →
Boehringer Ingelheim Pharma GmbH & Co. KG7 Mar 2014Human DrugsOn file

Sites inspected

Oishi Koseido Co., Ltd.Tosu, Japan2 insp.
Oishi Koseido Co., Ltd.Tosu, Japan1 insp.
Fresenius Kabi USA, LLCGrand Island, United States1 insp.
Boehringer Ingelheim Pharma GmbH & Co. KGIngelheim am Rhein, Germany1 insp.

Co-investigators

Investigators who share inspections with this person.

Vilmary Negron Rodriguez2 shared
Mindy M Chou1 shared

Full investigator report

Get the verbatim findings behind Erika E Englund's 20 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