# Intio Inc – FDA Inspection, Jan 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/intio-inc/2f8c2015-de23-4a86-8fa3-01f7c2469ec0
Source feed: FDA_Inspections

> FDA inspection 820040 of Intio Inc, January 18, 2013. Classification: Voluntary Action Indicated (VAI). 13 citations under 21 CFR parts 803 and 820.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 13

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