FDA Inspection 985187 — Sonoma Orthopedic Products, Inc.
The FDA completed an inspection of Sonoma Orthopedic Products, Inc. on Sep 15, 2016 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
- Sep 15, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Buffalo Grove, IL (United States)