# OMNIA SRL – FDA Inspection, Dec 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/omnia-srl/aa22d294-2ca7-4e4f-8315-51908cabb420
Source feed: FDA_Inspections

> FDA inspection 1000062 of OMNIA SRL, December 15, 2016. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000062
- Company Name: OMNIA SRL
- Inspection Date: 2016-12-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/omnia-srl/d2de86f5-913c-4bb4-8f27-e07f84ebdcea

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