FDA Investigator

Yangmin Ning

Latest inspection on record: Chicago, United States, November 2022 · records back to 2018

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 8 inspections across 8 sites are on record.
  • 4 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2022-11-16.

At a glance

Inspections

8

Sites

8

Observations

4

Career since

Nov 2018

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
XERIS PHARMACEUTICALS INC16 Nov 2022Human Drugs
Daiichi Sankyo, Inc.15 Jul 2022Human Drugs
AstraZeneca Pharmaceuticals LP27 Oct 2020Human Drugs
Ming-Shen Dai, M.D., Ph.D.27 Sep 2019Human DrugsOn file
Puma Biotechnology, Inc.24 May 2019Human DrugsView 483 →

Sites inspected

XERIS PHARMACEUTICALS INCChicago, United States1 insp.
Daiichi Sankyo, Inc.Basking Ridge, United States1 insp.
AstraZeneca Pharmaceuticals LPGaithersburg, United States1 insp.
Ming-Shen Dai, M.D., Ph.D.Taipei City, Taiwan1 insp.
Puma Biotechnology, Inc.Los Angeles, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Lee Hong Pai Scherf1 shared
David L Chon1 shared
Ni A Khin1 shared

Full investigator report

Get the verbatim findings behind Yangmin Ning's 4 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