# FDA Inspection 920497 - Everlife Medical Equipment Co., Ltd. - March 12, 2015

Source: https://www.keypedia.com/records/fda_inspections/everlife-medical-equipment-co-ltd/3b5b446f-b363-4c54-a0b8-9083491e1cdd
Source feed: FDA_Inspections

> FDA Inspection 920497 for Everlife Medical Equipment Co., Ltd. on March 12, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 920497
- Company Name: Everlife Medical Equipment Co., Ltd.
- Inspection Date: 2015-03-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1037883 - 2017-12-14](https://www.keypedia.com/records/fda_inspections/everlife-medical-equipment-co-ltd/05921e30-fb30-4ff3-aa87-97512283fe29)
- [FDA Inspection 920497 - 2015-03-12](https://www.keypedia.com/records/fda_inspections/everlife-medical-equipment-co-ltd/4a0c126f-3ace-4a84-a461-ac3b190be3e3)

Company: https://www.keypedia.com/companies/everlife-medical-equipment-co-ltd/3ecfa6b6-9ce5-424a-9a53-5fa3e97b5ad7

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