# Anteis Sa – FDA Inspection, Feb 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/anteis-sa/dec703e2-5878-45dd-ab25-9390a9be75e3
Source feed: FDA_Inspections

> FDA inspection 823159 of Anteis Sa, February 15, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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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)
- 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

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

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