FDA Inspection 1272818 — JIANGSU RIXIN MEDICAL EQUIPMENT CO., LTD
The FDA completed an inspection of JIANGSU RIXIN MEDICAL EQUIPMENT CO., LTD on May 29, 2025 in Suzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- May 29, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Suzhou (China)