# Omnitech Systems, Inc. – FDA Inspection, Jun 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/omnitech-systems-inc/fe54bdcd-6c7e-48ee-a371-287eb614866b
Source feed: FDA_Inspections

> FDA inspection 1060993 of Omnitech Systems, Inc., June 13, 2018. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060993
- Company Name: Omnitech Systems, Inc.
- Inspection Date: 2018-06-13
- 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: 0

## Related Documents

- [FDA Inspection 643042 - 2010-02-03](https://www.keypedia.com/records/fda_inspections/omnitech-systems-inc/bf19ac3a-3ede-47f1-8891-993bda5385b8)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/omnitech-systems-inc/5fb5b872-bdb4-4d9c-b72c-f70840a5dad5

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