# SUNWA LTD. – FDA Inspection, Jul 24, 2019

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

> FDA inspection 1098108 of SUNWA LTD., July 24, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sayeeda-hdabe/eaadc7cf-5f22-47c2-ba02-437efe0a5267)

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

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