FDA Investigator

Melkamu Getie Kebtie

Latest inspection on record: Chengdu, China, April 2026 · records back to 2017

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 45 inspections across 43 sites are on record.
  • 13 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2026-04-17.

At a glance

Inspections

45

Sites

43

Observations

13

Career since

Jan 2017

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Sichuan Huiyu Seacross Pharmaceutical Technology Co., Ltd.17 Apr 2026Human Drugs
Sichuan Huiyu Pharmaceutical Co., Ltd.16 Apr 2026Human Drugs
Regeneron Pharmaceuticals Inc10 Dec 2025Human Drugs
NORTHEAST BIOLAB5 Dec 2025Human DrugsOn file
Cohance Lifesciences (fka RA Chem Pharma Ltd.)31 Oct 2025Human DrugsOn file

Sites inspected

Sichuan Huiyu Seacross Pharmaceutical Technology Co., Ltd.Chengdu, China1 insp.
Regeneron Pharmaceuticals IncTarrytown, United States1 insp.
NORTHEAST BIOLABHamden, United States1 insp.
Cohance Lifesciences (fka RA Chem Pharma Ltd.)Hyderabad, India1 insp.

Co-investigators

Investigators who share inspections with this person.

Xikui Chen4 shared
Makini Cobourne-Duval4 shared
Amanda Lewin3 shared
Li-Hong Yeh3 shared
Nicola M Fenty-Stewart3 shared
Sarmistha Sanyal2 shared
Gopa Biswas2 shared

Full investigator report

Get the verbatim findings behind Melkamu Getie Kebtie's 13 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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