FDA Inspection 1256937 — OsteoLife Biomedical, LLC

OsteoLife Biomedical, LLC — FEI 3007936027

The FDA completed an inspection of OsteoLife Biomedical, LLC on December 11, 2024 in Jupiter, FL. 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
December 11, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Jupiter, FL (United States)