FDA Inspection 764359 — Osseolink USA, LLC

Osseolink USA, LLC — FEI 3008802367

The FDA completed an inspection of Osseolink USA, LLC on January 19, 2012 in Fort Washington, PA. 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
January 19, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Fort Washington, PA (United States)