FDA Inspection 736419 — Osiris Therapeutics Inc

Osiris Therapeutics Inc — FEI 3006638648

The FDA completed an inspection of Osiris Therapeutics Inc on July 14, 2011 in Columbia, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 14, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Columbia, MD (United States)