# Elucid Bioimaging Inc. – FDA Inspection, Apr 2, 2019

Source: https://www.keypedia.com/records/fda_inspections/elucid-bioimaging-inc/ec580ff8-78d7-4414-8d21-2ab554440ff3
Source feed: FDA_Inspections

> FDA inspection 1084923 of Elucid Bioimaging Inc., April 02, 2019. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1084923
- Company Name: Elucid Bioimaging Inc.
- Inspection Date: 2019-04-02
- 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: 5

## Related Documents

- [FDA Inspection 1308272 - 2026-03-20](https://www.keypedia.com/records/fda_inspections/elucid-bioimaging-inc/a0be587d-6b31-48a7-8101-de82c1cdef3e)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/stephen-c-smith/426649fa-0e5b-4b35-ba41-636512a06a48)

Company: https://www.keypedia.com/companies/elucid-bioimaging-inc/bbfec801-76d5-4377-b57b-0045ffb4bd7f

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