# Emerge Diagnostics Inc. – FDA Inspection, Apr 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/emerge-diagnostics-inc/a7fb1db4-b0b5-439f-8ab0-3c7a45b86915
Source feed: FDA_Inspections

> FDA inspection 1088818 of Emerge Diagnostics Inc., April 26, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088818
- Company Name: Emerge Diagnostics Inc.
- Inspection Date: 2019-04-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1245806 - 2024-08-08](https://www.keypedia.com/records/fda_inspections/emerge-diagnostics-inc/60f57c2c-a2d6-43c4-8d1d-ecde5fe7bd6e)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)
- [Issuing Officer](https://www.keypedia.com/people/juanj-wu/0d3e8970-b524-49f6-a307-079091b3c91d)

Company: https://www.keypedia.com/companies/emerge-diagnostics-inc/ba2abd8f-f460-4e69-b687-3e418042da6b

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