FDA Inspection 1325770 — Zhejiang Innuovo Rehabilitation Devices Co. Ltd.
The FDA completed an inspection of Zhejiang Innuovo Rehabilitation Devices Co. Ltd. on Jun 4, 2026 in Jinhua. 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
- Jun 4, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Jinhua (China)