# FDA Inspection 1014455 - iMed Technology, Inc - June 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/imed-technology-inc/ca0f9f28-cb1f-4117-b0dc-9145bc5039cb
Source feed: FDA_Inspections

> FDA Inspection 1014455 for iMed Technology, Inc on June 16, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014455
- Company Name: iMed Technology, Inc
- Inspection Date: 2017-06-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/imed-technology-inc/08272093-861d-4968-a375-dd65280700e4

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