# ANT North America Inc – FDA Inspection, Jun 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/ant-north-america-inc/29157f8c-4ef9-48ba-aed5-2fdf9eb8e9ae
Source feed: FDA_Inspections

> FDA inspection 839578 of ANT North America Inc, June 10, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839578
- Company Name: ANT North America Inc
- Inspection Date: 2013-06-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 811279 - 2012-12-07](https://www.keypedia.com/records/fda_inspections/ant-north-america-inc/460b56e1-b0bc-4d0d-803f-d49b476d1e90)

Company: https://www.keypedia.com/companies/ant-north-america-inc/400d3ae6-5a8b-4f48-8501-aaacd17c1015

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