FDA Inspection 643401 — Orthofix U.S. LLC

Orthofix U.S. LLC — FEI 2183449

The FDA completed an inspection of Orthofix U.S. LLC on December 16, 2009 in Lewisville, TX. 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 16, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Lewisville, TX (United States)