FDA Investigator

Laurimer Kuilan-Torres

Latest inspection on record: Dortmund, Germany, March 2026 · records back to 2015

Human DrugsFoods & CosmeticsAnimal Drugs & FeedsMedical Devices & Rad Health

FDA inspection record · Last updated July 12, 2026

Overview

  • 77 inspections across 73 sites are on record.
  • 109 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-03-26.

At a glance

Inspections

77

Sites

73

Observations

109

Career since

May 2015

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
ProtaGene GmbH26 Mar 2026Human Drugs
Merck Serono SA25 Nov 2025Human Drugs
Emergent BioSolutions Canada Inc.27 Aug 2025Human DrugsOn file
Aurolife Pharma LLC10 Apr 2025Human DrugsOn file
Ionetix Corporation6 Feb 2025Human DrugsOn file

Sites inspected

ProtaGene GmbHDortmund, Germany1 insp.
Merck Serono SAAubonne, Switzerland1 insp.
Emergent BioSolutions Canada Inc.Winnipeg, Canada1 insp.
Aurolife Pharma LLCDurham, United States1 insp.
Ionetix CorporationKnoxville, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Vilmary Negron Rodriguez5 shared
Yiwei Li2 shared
Lane V Christensen2 shared
Ariel Cruz Figueroa2 shared
Binh T Nguyen2 shared
Djamila Harouaka2 shared

Full investigator report

Get the verbatim findings behind Laurimer Kuilan-Torres' 109 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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