FDA Inspection 1279413 — Sanguina, Inc.
The FDA completed an inspection of Sanguina, Inc. on Aug 20, 2025 in Peachtree Corners, GA. 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
- Aug 20, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Peachtree Corners, GA (United States)