# FDA Inspection 891123 - VIVEVE DENVER - August 01, 2014

Source: https://www.keypedia.com/records/fda_inspections/viveve-denver/bf8c6433-0d91-4e39-b9aa-5217bdce991e
Source feed: FDA_Inspections

> FDA Inspection 891123 for VIVEVE DENVER on August 01, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891123
- Company Name: VIVEVE DENVER
- Inspection Date: 2014-08-01
- 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 891123 - 2014-08-01](https://www.keypedia.com/records/fda_inspections/viveve-denver/8d08b996-2f18-4995-9deb-5be6a7883c6c)

Company: https://www.keypedia.com/companies/viveve-denver/1a63ed0c-57f1-4e8a-bab9-a52346efb24a

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