# Zenith Technology Corporation, Ltd. – FDA Inspection, Apr 28, 2023

Source: https://www.keypedia.com/records/fda_inspections/zenith-technology-corporation-ltd/f5cae597-4e62-47c8-8dd0-c799f05a90ed
Source feed: FDA_Inspections

> FDA inspection 1205972 of Zenith Technology Corporation, Ltd., April 28, 2023. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1205972
- Company Name: Zenith Technology Corporation, Ltd.
- Inspection Date: 2023-04-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1118376 - 2020-01-30
- [FDA Inspection 1121501 - 2020-01-16](https://www.keypedia.com/records/fda_inspections/zenith-technology-corporation-ltd/9c61cfdb-ecae-456a-8d41-fa3b96517f6a)
- FDA Inspection 1045698 - 2016-12-13
- FDA Inspection 995060 - 2016-11-21

## Related Officers

- [Investigator](https://www.keypedia.com/people/richard-w-berning/4637e321-8803-4fcf-911f-bbc810c3487d)

Company: https://www.keypedia.com/companies/zenith-technology-corporation-ltd/12515af0-3e56-44a0-bf61-ea673759d721

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c