# FDA Inspection 809981 - Primo Medical Group, Inc - December 10, 2012

Source: https://www.keypedia.com/records/fda_inspections/primo-medical-group-inc/9e38e375-4030-4782-b6f5-d948e800ae7b
Source feed: FDA_Inspections

> FDA Inspection 809981 for Primo Medical Group, Inc on December 10, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 809981
- Company Name: Primo Medical Group, Inc
- Inspection Date: 2012-12-10
- 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/primo-medical-group-inc/707d0aea-9ae4-4c83-9f5f-20d1b43f586b

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