# FDA Inspection 1238306 - Citieffe Srl - February 15, 2024

Source: https://www.keypedia.com/records/fda_inspections/citieffe-srl/5a50de20-1d15-4645-8629-10411afe24d4
Source feed: FDA_Inspections

> FDA Inspection 1238306 for Citieffe Srl on February 15, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1238306
- Company Name: Citieffe Srl
- Inspection Date: 2024-02-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/citieffe-srl/22ed3ebc-567f-4f32-bf32-12e8b41c1346

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