FDA Inspection 1065410 — Orthobone, Inc.

Orthobone, Inc. — FEI 3008410332

The FDA completed an inspection of Orthobone, Inc. on August 16, 2018 in San Juan, PR. 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 16, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
San Juan, PR (United States)