FDA Inspection 1290462 — Nutek Bravo, LLC.
The FDA completed an inspection of Nutek Bravo, LLC. on Oct 30, 2025 in Hayward, 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
- Oct 30, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Hayward, CA (United States)