# Anuncia, Inc. – FDA Inspection, Nov 14, 2018

Source: https://www.keypedia.com/records/fda_inspections/anuncia-inc/9d1da369-2110-4582-b613-57add8157da0
Source feed: FDA_Inspections

> FDA inspection 1071623 of Anuncia, Inc., November 14, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1071623
- Company Name: Anuncia, Inc.
- Inspection Date: 2018-11-14
- 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: 1

## Related Officers

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

Company: https://www.keypedia.com/companies/anuncia-inc/0dfd843a-4b05-44bc-bdea-493d9f9dacb0

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