# FDA Inspection 925740 - Helio USA Inc - May 12, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/helio-usa-inc/af6aa59a-c483-4899-b73e-ba1f644b88eb
Source feed: FDA_Inspections

> FDA Inspection 925740 for Helio USA Inc on May 12, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 925740
- Company Name: Helio USA Inc
- Inspection Date: 2015-05-12
- 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/helio-usa-inc/5c2e6761-b856-452e-8b37-2ecc0aa37dc4

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