FDA Inspection 1027565 — Synvasive Technology, Inc.
The FDA completed an inspection of Synvasive Technology, Inc. on May 4, 2017 in Reno, NV. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- May 4, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Reno, NV (United States)