# Zenith Diagnostics – FDA Inspection, Nov 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/zenith-diagnostics/cc0b9a9b-3b79-45a8-86dd-68fe348a2d11
Source feed: FDA_Inspections

> FDA inspection 1072319 of Zenith Diagnostics, November 20, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1072319
- Company Name: Zenith Diagnostics
- Inspection Date: 2018-11-20
- 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/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/zenith-diagnostics/041cf325-8031-4fbe-937b-b2327a163777

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