# FDA Inspection 1098108 - SUNWA LTD. - July 24, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/sunwa-ltd/7075a0bd-c4bf-48d9-8175-144677dafbb2
Source feed: FDA_Inspections

> FDA Inspection 1098108 for SUNWA LTD. on July 24, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098108
- Company Name: SUNWA LTD.
- Inspection Date: 2019-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/sunwa-ltd/9a86f70d-d185-4092-a9ac-a3d5da0f27c3

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