# Clarity Diagnostics, LLC – FDA Inspection, May 8, 2019

Source: https://www.keypedia.com/records/fda_inspections/clarity-diagnostics-llc/92c79206-5d81-476d-9d90-f85493d2e3c2
Source feed: FDA_Inspections

> FDA inspection 1088913 of Clarity Diagnostics, LLC, May 08, 2019. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803, 806 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088913
- Company Name: Clarity Diagnostics, LLC
- Inspection Date: 2019-05-08
- 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: 6

## Related Documents

- FDA Inspection 1169763 - 2022-04-06
- [FDA Inspection 833184 - 2013-05-23](https://www.keypedia.com/records/fda_inspections/clarity-diagnostics-llc/ba590d06-8325-47ee-93f2-f5df0fc961e1)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

Company: https://www.keypedia.com/companies/clarity-diagnostics-llc/d00e9188-408f-49ef-8fb8-1790097a42be

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