# IMANI – FDA Inspection, Mar 22, 2023

Source: https://www.keypedia.com/records/fda_inspections/imani/d0150101-457d-4893-85b7-1f505825fa16
Source feed: FDA_Inspections

> FDA inspection 1200437 of IMANI, March 22, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200437
- Company Name: IMANI
- Inspection Date: 2023-03-22
- 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: 2

## Related Officers

- [Investigator](https://www.keypedia.com/people/preston-m-lee/e44adac3-a915-4bfb-8b06-a41ea5803358)

Company: https://www.keypedia.com/companies/imani/7d7bbafd-d62e-4168-b0bd-96e229499981

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