FDA Inspection 818402 — Sonoma Orthopedic Products, Inc.

Sonoma Orthopedic Products, Inc. — FEI 3007038372

The FDA completed an inspection of Sonoma Orthopedic Products, Inc. on Feb 13, 2013 in Buffalo Grove, IL. 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
Feb 13, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Buffalo Grove, IL (United States)