# Domico Med-Device Llc – FDA Inspection, Nov 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/domico-med-device-llc/6327ac53-e106-4a01-8c23-dd937040609a
Source feed: FDA_Inspections

> FDA inspection 992489 of Domico Med-Device Llc, November 10, 2016. Classification: No Action Indicated (NAI). 4 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: 992489
- Company Name: Domico Med-Device Llc
- Inspection Date: 2016-11-10
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1316708 - 2026-05-12](https://www.keypedia.com/records/fda_inspections/domico-med-device-llc/b29118fd-b3b8-4a3a-a61c-cfd327a05806)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/domico-med-device-llc/a96d3c85-e474-46dc-a86f-629bf3588679

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