FDA Inspection 783031 — Orthoscan, Inc.

Orthoscan, Inc. — FEI 3005254598

The FDA completed an inspection of Orthoscan, Inc. on May 24, 2012 in Scottsdale, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 24, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Scottsdale, AZ (United States)