# FDA Inspection 988533 - Caremaster Technology (Hk) Group Co., Ltd - September 22, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/caremaster-technology-hk-group-co-ltd/fbe340b6-b8a6-4d5d-8f7e-106721518be2/
Source feed: FDA_Inspections

> FDA Inspection 988533 for Caremaster Technology (Hk) Group Co., Ltd on September 22, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988533
- Company Name: Caremaster Technology (Hk) Group Co., Ltd
- Inspection Date: 2016-09-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 988533 - 2016-09-22](https://www.globalkeysolutions.net/api/records/fda_inspections/caremaster-technology-hk-group-co-ltd/e7e5f794-b9a1-49ca-ab49-17b894390529/)

Company: https://www.globalkeysolutions.net/companies/caremaster-technology-hk-group-co-ltd/1d3f1ccb-323a-4f6c-8090-90fa5c874420

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