# Senzime AB – FDA Inspection, Jan 18, 2024

Source: https://www.keypedia.com/records/fda_inspections/senzime-ab/c6884f3d-68a3-487f-a828-8e8bf2eb5e88
Source feed: FDA_Inspections

> FDA inspection 1227196 of Senzime AB, January 18, 2024. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1227196
- Company Name: Senzime AB
- Inspection Date: 2024-01-18
- 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: 3

## Related Officers

- [Mary A. Millner](https://www.keypedia.com/people/mary-a-millner/bd8911cf-849d-41d2-ae12-dd4bad66e798)

Company: https://www.keypedia.com/companies/senzime-ab/1df1a410-852f-4e44-83da-8bd8e81889fd

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