# DOMINO S.R.L. – FDA Inspection, Sep 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/domino-srl/d54b5579-8666-472b-9c03-da9c937261bc
Source feed: FDA_Inspections

> FDA inspection 1027961 of DOMINO S.R.L., September 14, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1027961
- Company Name: DOMINO S.R.L.
- Inspection Date: 2017-09-14
- 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 1259259 - 2024-12-19
- [FDA Inspection 887570 - 2014-06-05](https://www.keypedia.com/records/fda_inspections/domino-srl/356aa289-6296-407d-a1ce-f3f071d026f4)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/domino-srl/29bdabf5-cc6c-4dba-86bc-d9d5b08fd3ac

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