# FDA Inspection 823159 - Anteis Sa - February 15, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/anteis-sa/66d17e9d-ce20-4103-92ed-d9a3934aa3b8
Source feed: FDA_Inspections

> FDA Inspection 823159 for Anteis Sa on February 15, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 823159
- Company Name: Anteis Sa
- Inspection Date: 2013-02-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/anteis-sa/7c680f18-c418-4a1a-9de4-a89d5391d718

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