FDA Investigator

Geoffrey K Kilili

Latest inspection on record: Gurugram, India, May 2026 · records back to 2016

Human DrugsMedical Devices & Rad HealthBiologicsFoods & CosmeticsAnimal Drugs & Feeds

FDA inspection record · Last updated July 12, 2026

Overview

  • 102 inspections across 98 sites are on record.
  • 161 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-05-08.

At a glance

Inspections

102

Sites

98

Observations

161

Career since

Mar 2016

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited)8 May 2026Human DrugsOn file
Axxelent Pharma Science Private Limited17 Apr 2026Human DrugsOn file
Aarti Pharmalabs Limited27 Mar 2026Human DrugsOn file
Lupin Limited7 Mar 2026Human DrugsOn file
PETNET Solutions, Inc.3 Feb 2026Human DrugsOn file

Sites inspected

Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited)Gurugram, India1 insp.
Axxelent Pharma Science Private LimitedSri City, Tirupati, India1 insp.
Aarti Pharmalabs LimitedPalghar, India1 insp.
Lupin LimitedAnkleshwar, India1 insp.
PETNET Solutions, Inc.Cincinnati, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Craig T Rybus4 shared
Karen M Cooper4 shared
Jacob G Lutz2 shared
Cheryl A Grandinetti2 shared
Yvette M Lacour-Davis2 shared
Marcia A Worley2 shared

Full investigator report

Get the verbatim findings behind Geoffrey K Kilili's 161 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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