FDA Inspection 1028926 — OsteoLife Biomedical, LLC

OsteoLife Biomedical, LLC — FEI 3007936027

The FDA completed an inspection of OsteoLife Biomedical, LLC on August 15, 2017 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
August 15, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Jupiter, FL (United States)