# Genway Biotech Inc. – FDA Inspection, Jun 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 of Genway Biotech Inc., June 14, 2018. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1056861
- Company Name: Genway Biotech Inc.
- Inspection Date: 2018-06-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sonya-l-karsik/c24603b9-5ca0-46f5-861a-b367155b0def)

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