# FDA Inspection 1200396 - Artiglass Srl - February 09, 2023

Source: https://www.keypedia.com/records/fda_inspections/artiglass-srl/7ebf01a3-ce50-4667-9905-29e0f134f2f6
Source feed: FDA_Inspections

> FDA Inspection 1200396 for Artiglass Srl on February 09, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200396
- Company Name: Artiglass Srl
- Inspection Date: 2023-02-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1200396 - 2023-02-09](https://www.keypedia.com/records/fda_inspections/artiglass-srl/0831c632-a239-45c5-8968-d3e08c3f4bec)

Company: https://www.keypedia.com/companies/artiglass-srl/031f3a49-da22-42ce-969b-a87a380965e9

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