# FDA Inspection 1004833 - ZenTech SA - February 09, 2017

Source: https://www.keypedia.com/records/fda_inspections/zentech-sa/7b62b5f5-3397-4548-8bbe-3975ca7ebb96
Source feed: FDA_Inspections

> FDA Inspection 1004833 for ZenTech SA on February 09, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004833
- Company Name: ZenTech SA
- Inspection Date: 2017-02-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1004833 - 2017-02-09](https://www.keypedia.com/records/fda_inspections/zentech-sa/99e1c76b-c638-453d-ae5c-9ebf0d9dac0e)

Company: https://www.keypedia.com/companies/zentech-sa/5739fb24-75c2-45f8-83ec-079872fd32bb

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