# Omnitech Systems, Inc. – FDA Inspection, Feb 3, 2010

Source: https://www.keypedia.com/records/fda_inspections/omnitech-systems-inc/bf19ac3a-3ede-47f1-8891-993bda5385b8
Source feed: FDA_Inspections

> FDA inspection 643042 of Omnitech Systems, Inc., February 03, 2010. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 643042
- Company Name: Omnitech Systems, Inc.
- Inspection Date: 2010-02-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1060993 - 2018-06-13](https://www.keypedia.com/records/fda_inspections/omnitech-systems-inc/fe54bdcd-6c7e-48ee-a371-287eb614866b)

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