# FDA Inspection 1026110 - Sunder Biomedical Tech Co., Ltd. - September 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/sunder-biomedical-tech-co-ltd/9adea787-ec78-42c8-83a9-0fdf4f08a087
Source feed: FDA_Inspections

> FDA Inspection 1026110 for Sunder Biomedical Tech Co., Ltd. on September 13, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026110
- Company Name: Sunder Biomedical Tech Co., Ltd.
- Inspection Date: 2017-09-13
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1026110 - 2017-09-13](https://www.keypedia.com/records/fda_inspections/sunder-biomedical-tech-co-ltd/56ca8bf5-d72d-4d44-a781-7b5155759c47)

Company: https://www.keypedia.com/companies/sunder-biomedical-tech-co-ltd/0b6f0af6-b8fd-4c10-9140-f3cf6a4abc7c

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