# FDA Inspection 1088144 - SUNTECH MEDICAL DEVICES (SHENZHEN) CO., LTD. - November 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/suntech-medical-devices-shenzhen-co-ltd/55ecc670-2529-44e2-b689-e6b5c30dbc68
Source feed: FDA_Inspections

> FDA Inspection 1088144 for SUNTECH MEDICAL DEVICES (SHENZHEN) CO., LTD. on November 29, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088144
- Company Name: SUNTECH MEDICAL DEVICES (SHENZHEN) CO., LTD.
- Inspection Date: 2018-11-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 886473 - 2014-06-12](https://www.keypedia.com/records/fda_inspections/suntech-medical-devices-shenzhen-co-ltd/2a61894f-1312-4807-8b19-ed276857b6eb)

Company: https://www.keypedia.com/companies/suntech-medical-devices-shenzhen-co-ltd/d01bf505-cd5c-446e-bcec-90be25c86021

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7