FDA Inspection 650231 — Ortho One, Inc

Ortho One, Inc — FEI 3004627926

The FDA completed an inspection of Ortho One, Inc on Mar 4, 2010 in Tucson, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 4, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Tucson, AZ (United States)