FDA Inspection 1059665 — Veniti, Inc.
The FDA completed an inspection of Veniti, Inc. on Jul 20, 2018 in Fremont, 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
- Jul 20, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Fremont, CA (United States)