# FDA Inspection 922461 - Shenzhen Homed Medical Device Co., Ltd. - March 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-homed-medical-device-co-ltd/cbb32347-3b6b-405f-8b9c-bc191421c6a5
Source feed: FDA_Inspections

> FDA Inspection 922461 for Shenzhen Homed Medical Device Co., Ltd. on March 26, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 922461
- Company Name: Shenzhen Homed Medical Device Co., Ltd.
- Inspection Date: 2015-03-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 922461 - 2015-03-26](https://www.keypedia.com/records/fda_inspections/shenzhen-homed-medical-device-co-ltd/919e71ef-c9b8-423d-a77d-03f772c84b12)

Company: https://www.keypedia.com/companies/shenzhen-homed-medical-device-co-ltd/515ea877-23c4-4814-b5d6-7f484e89608c

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