FDA Inspection 1057926 — ReNovo, Inc.
The FDA completed an inspection of ReNovo, Inc. on Jun 21, 2018 in Bend, OR. 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
- Jun 21, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Bend, OR (United States)