FDA Inspection 904191 — Dornoch Medical Systems Inc
The FDA completed an inspection of Dornoch Medical Systems Inc on Nov 19, 2014 in Riverside, MO. 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
- Nov 19, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Riverside, MO (United States)