# FDA Inspection 1080023 - DRE Medical Group Inc - February 21, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/dre-medical-group-inc/fcfb99f6-2971-4fd1-a845-ac8deb466401/
Source feed: FDA_Inspections

> FDA Inspection 1080023 for DRE Medical Group Inc on February 21, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1080023
- Company Name: DRE Medical Group Inc
- Inspection Date: 2019-02-21
- 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.globalkeysolutions.net/companies/dre-medical-group-inc/e50ac3a0-76b3-4f86-b6a2-aa89f3216212

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