FDA Inspection 1297228 — SUZHOU JENITEK PRECISION DEVICE CO.,LTD.
The FDA completed an inspection of SUZHOU JENITEK PRECISION DEVICE CO.,LTD. on Dec 11, 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
- Dec 11, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Suzhou (China)