# ADRIA SRL – FDA Inspection, Mar 16, 2023

Source: https://www.keypedia.com/records/fda_inspections/adria-srl/be7d38af-effe-4840-b253-7c6061d3c845
Source feed: FDA_Inspections

> FDA inspection 1200410 of ADRIA SRL, March 16, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200410
- Company Name: ADRIA SRL
- Inspection Date: 2023-03-16
- 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: 2

## Related Documents

- [FDA Inspection 1293884 - 2025-12-04](https://www.keypedia.com/records/fda_inspections/adria-srl/948d12a4-dfce-4b34-82f1-10930671ecdd)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maryam-tabatabaie/b792042d-e296-446d-90a9-d30c8f635506)

Company: https://www.keypedia.com/companies/adria-srl/8b0c5e3a-f2d5-4838-a8fa-7e3f885a5497

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