# FDA Inspection 1009910 - Omni-Guide Holdings, Inc. - May 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/omni-guide-holdings-inc/7c90fe8f-cbcf-417a-a4a5-00bdac37f82d
Source feed: FDA_Inspections

> FDA Inspection 1009910 for Omni-Guide Holdings, Inc. on May 02, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009910
- Company Name: Omni-Guide Holdings, Inc.
- Inspection Date: 2017-05-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/omni-guide-holdings-inc/5e155363-4080-4984-aa63-81ad46877ef5

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