# FDA Inspection 1000062 - OMNIA SRL - December 15, 2016

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

> FDA Inspection 1000062 for OMNIA SRL on December 15, 2016. Classification: No Action Indicated (NAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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