# ZenTech SA – FDA Inspection, Feb 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/zentech-sa/99e1c76b-c638-453d-ae5c-9ebf0d9dac0e
Source feed: FDA_Inspections

> FDA inspection 1004833 of ZenTech SA, February 09, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- Issuing Officer

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