# FDA Inspection 1040215 - Velano Vascular - January 29, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/velano-vascular/b026575c-209e-437b-a93b-6b247f0de1a6
Source feed: FDA_Inspections

> FDA Inspection 1040215 for Velano Vascular on January 29, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040215
- Company Name: Velano Vascular
- Inspection Date: 2018-01-29
- 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 1040215 - 2018-01-29](https://www.globalkeysolutions.net/records/fda_inspections/velano-vascular/50cd1986-60aa-4a25-a82e-38a8e6c493c5)

Company: https://www.globalkeysolutions.net/companies/velano-vascular/a9c17d44-f7c4-4599-a0f5-ce15250a6522

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