FDA Inspection 955250 — Tecfen Medical
The FDA completed an inspection of Tecfen Medical on Jan 5, 2016 in Santa Barbara, CA. 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
- Jan 5, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Santa Barbara, CA (United States)