# FDA Inspection 1056861 - Genway Biotech Inc. - June 14, 2018

Source: https://www.keypedia.com/records/fda_inspections/genway-biotech-inc/85cd4296-a9a6-400c-bb7e-c787d1ee5b27
Source feed: FDA_Inspections

> FDA Inspection 1056861 for Genway Biotech Inc. on June 14, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056861
- Company Name: Genway Biotech Inc.
- Inspection Date: 2018-06-14
- 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 1056861 - 2018-06-14](https://www.keypedia.com/records/fda_inspections/genway-biotech-inc/29622f43-35c3-48be-a5f5-03e261865222)

Company: https://www.keypedia.com/companies/genway-biotech-inc/b109528d-2e6b-4231-94d4-c7e1994e2610

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