# FDA Inspection 1297228 - SUZHOU JENITEK PRECISION DEVICE CO.,LTD. - December 11, 2025

Source: https://www.keypedia.com/records/fda_inspections/suzhou-jenitek-precision-device-coltd/b607915d-6f1a-4eee-b78f-3842b10e771e
Source feed: FDA_Inspections

> FDA Inspection 1297228 for SUZHOU JENITEK PRECISION DEVICE CO.,LTD. on December 11, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1297228
- Company Name: SUZHOU JENITEK PRECISION DEVICE CO.,LTD.
- Inspection Date: 2025-12-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1297228 - 2025-12-11](https://www.keypedia.com/records/fda_inspections/suzhou-jenitek-precision-device-coltd/e0347e10-c6a1-4a61-afcf-ccc298f22d90)
- [FDA Inspection 1297228 - 2025-12-11](https://www.keypedia.com/records/fda_inspections/suzhou-jenitek-precision-device-coltd/bc220bec-7c5d-424c-9603-dac9135c442a)

Company: https://www.keypedia.com/companies/suzhou-jenitek-precision-device-coltd/ffd320ba-1d9d-4ccb-8d08-d41f4f78dd06