# Omni Components Corporation – FDA Inspection, Aug 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/omni-components-corporation/6c4ee3b2-51d7-4713-bb63-cbe95cc90bc1
Source feed: FDA_Inspections

> FDA inspection 1023693 of Omni Components Corporation, August 31, 2017. Classification: No Action Indicated (NAI). 5 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023693
- Company Name: Omni Components Corporation
- Inspection Date: 2017-08-31
- 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: 5

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/omni-components-corporation/6d096827-6304-43af-8f91-acf43cf16fc7

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