# Hongrita Plastics (Shenzhen) Ltd. – FDA Inspection, Feb 1, 2018

Source: https://www.keypedia.com/records/fda_inspections/hongrita-plastics-shenzhen-ltd/e9ddbda8-13c2-4c21-a9ab-59e80caef032
Source feed: FDA_Inspections

> FDA inspection 1042415 of Hongrita Plastics (Shenzhen) Ltd., February 01, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042415
- Company Name: Hongrita Plastics (Shenzhen) Ltd.
- Inspection Date: 2018-02-01
- 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: 1

## Related Officers

- [Company Rep](https://www.keypedia.com/people/mark-e-chan/2a5a3abf-96f6-4ceb-b87d-379ed5c6f47e)

Company: https://www.keypedia.com/companies/hongrita-plastics-shenzhen-ltd/793ac6fd-2e17-4283-adb3-e8daddbb13b9

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