# FDA Inspection 1060993 - Omnitech Systems, Inc. - June 13, 2018

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

> FDA Inspection 1060993 for Omnitech Systems, Inc. on June 13, 2018. Classification: No Action Indicated (NAI).

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

## Related Documents

- [FDA Inspection 1060993 - 2018-06-13](https://www.globalkeysolutions.net/api/records/fda_inspections/omnitech-systems-inc/ce301d0f-a00f-42a6-8fe5-bbdb7773a2b9/)
- [FDA Inspection 643042 - 2010-02-03](https://www.globalkeysolutions.net/api/records/fda_inspections/omnitech-systems-inc/80d5fc9f-5758-43d1-92be-d0c9ba25a442/)
- [FDA Inspection 643042 - 2010-02-03](https://www.globalkeysolutions.net/api/records/fda_inspections/omnitech-systems-inc/bf19ac3a-3ede-47f1-8891-993bda5385b8/)

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

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