# FDA Inspection 630082 - Anteis Sa - November 04, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/anteis-sa/6f368d04-c572-468a-b594-1b2473e8688b
Source feed: FDA_Inspections

> FDA Inspection 630082 for Anteis Sa on November 04, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 630082
- Company Name: Anteis Sa
- Inspection Date: 2009-11-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1305880 - 2026-02-25](https://www.globalkeysolutions.net/records/fda_inspections/anteis-sa/637b0dad-52af-4ed5-857e-73293b7fcc8a)
- [FDA Inspection 1305880 - 2026-02-25](https://www.globalkeysolutions.net/records/fda_inspections/anteis-sa/4e816ed8-0ebe-45cb-8694-9477191d3c8b)
- [FDA Inspection 823159 - 2013-02-15](https://www.globalkeysolutions.net/records/fda_inspections/anteis-sa/66d17e9d-ce20-4103-92ed-d9a3934aa3b8)
- [FDA Inspection 823159 - 2013-02-15](https://www.globalkeysolutions.net/records/fda_inspections/anteis-sa/dec703e2-5878-45dd-ab25-9390a9be75e3)
- [FDA Inspection 630082 - 2009-11-04](https://www.globalkeysolutions.net/records/fda_inspections/anteis-sa/4415798e-5d0b-40bb-aecc-43c8b2683afb)

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