FDA Inspection 1231015 — Vitalconnect Inc.
The FDA completed an inspection of Vitalconnect Inc. on February 15, 2024 in San Jose, CA. 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
- February 15, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- San Jose, CA (United States)