# Omarc Llc – FDA Inspection, Oct 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/omarc-llc/5f0baaa4-1887-432a-9407-b135e863a146
Source feed: FDA_Inspections

> FDA inspection 991802 of Omarc Llc, October 28, 2016. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991802
- Company Name: Omarc Llc
- Inspection Date: 2016-10-28
- 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: 2

## Related Documents

- FDA Inspection 1150127 - 2021-08-11
- [FDA Inspection 796293 - 2012-08-24](https://www.keypedia.com/records/fda_inspections/omarc-llc/daa3decf-2669-44a9-bdc4-697f724155ff)
- [FDA Inspection 769507 - 2012-03-01](https://www.keypedia.com/records/fda_inspections/omarc-llc/6f5dabb1-d6e1-42ac-b257-1e84e22be7cc)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/laureen-m-geniusz/759a858e-e3f3-4c48-8194-9804c7ab2a7b)

Company: https://www.keypedia.com/companies/omarc-llc/2021bed7-6898-4a3b-b023-8d4e9a122a85

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