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FDA Inspection
•Stephane Leung Wai Sang, MD•February 24, 2026

Stephane Leung Wai Sang, MD – FDA Inspection, Feb 24, 2026

Record Details

This FDA Inspection record concerns Stephane Leung Wai Sang, MD, with an inspection on February 24, 2026, issued by the Detroit District Office, covering medical devices & rad health.

Company
Stephane Leung Wai Sang, MD
Inspection Date
February 24, 2026
Product Type
Medical Devices & Rad Health
Office
Detroit District Office
Person
  • Chelsea W. Lamm (Company Rep)
View Company Profile

ID · 183ffaf2-101a-43a7-b841-3d91a1f38ac8

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1304318
FDA center
Medical Devices & Rad Health
Project area
Product Evaluation: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations

Full citation text and observation details available on the Dashboard.

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