FDA Inspection 1259206 — Vitalgo, Inc.
The FDA completed an inspection of Vitalgo, Inc. on Dec 13, 2024 in Miramar, FL. 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
- Dec 13, 2024
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Miramar, FL (United States)