# FDA Inspection 820040 - Intio Inc - January 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/intio-inc/0ac8eb30-be50-4b52-a225-89b01dfee1ee
Source feed: FDA_Inspections

> FDA Inspection 820040 for Intio Inc on January 18, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820040
- Company Name: Intio Inc
- Inspection Date: 2013-01-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 820040 - 2013-01-18](https://www.keypedia.com/records/fda_inspections/intio-inc/2f8c2015-de23-4a86-8fa3-01f7c2469ec0)

Company: https://www.keypedia.com/companies/intio-inc/75d7d2f4-c599-403c-a5e4-5a3719772c15

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