# FDA Inspection 1072319 - Zenith Diagnostics (dba) Vertex Diagnostics LLC - November 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/zenith-diagnostics-dba-vertex-diagnostics-llc/51424784-d7be-465f-8e8a-06c207901a04
Source feed: FDA_Inspections

> FDA Inspection 1072319 for Zenith Diagnostics (dba) Vertex Diagnostics LLC on November 20, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1072319
- Company Name: Zenith Diagnostics (dba) Vertex Diagnostics LLC
- Inspection Date: 2018-11-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1072319 - 2018-11-20](https://www.globalkeysolutions.net/records/fda_inspections/zenith-diagnostics-dba-vertex-diagnostics-llc/cc0b9a9b-3b79-45a8-86dd-68fe348a2d11)

Company: https://www.globalkeysolutions.net/companies/zenith-diagnostics-dba-vertex-diagnostics-llc/041cf325-8031-4fbe-937b-b2327a163777

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