FDA Inspection 1254554 — Longeviti Neuro Solutions LLC
The FDA completed an inspection of Longeviti Neuro Solutions LLC on Nov 15, 2024 in Baltimore, MD. 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
- Nov 15, 2024
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Baltimore, MD (United States)