FDA Inspection 1284618 — Osiris Therapeutics Inc

Osiris Therapeutics Inc — FEI 3006638648

The FDA completed an inspection of Osiris Therapeutics Inc on Aug 27, 2026 in Columbia, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 27, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Columbia, MD (United States)