# FDA Inspection 783860 - Vivatek Inc - April 17, 2012

Source: https://www.keypedia.com/records/fda_inspections/vivatek-inc/8ce4dc3e-f388-41bf-a8cd-ed22d238f0ab
Source feed: FDA_Inspections

> FDA Inspection 783860 for Vivatek Inc on April 17, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 783860
- Company Name: Vivatek Inc
- Inspection Date: 2012-04-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/vivatek-inc/f67cf562-60bf-4822-97b1-d3324f741c34

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