FDA Inspection 1215912 — Intravu, Inc.
The FDA completed an inspection of Intravu, Inc. on Jul 7, 2023 in Redwood City, 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 7, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Redwood City, CA (United States)