# FDA Inspection 1018581 - VIANT PUERTO RICO, INC - June 02, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/viant-puerto-rico-inc/3cf072d0-51fc-45bf-9fc3-7527cdfe3e6d
Source feed: FDA_Inspections

> FDA Inspection 1018581 for VIANT PUERTO RICO, INC on June 02, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1018581
- Company Name: VIANT PUERTO RICO, INC
- Inspection Date: 2017-06-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1296408 - 2025-12-19](https://www.globalkeysolutions.net/records/fda_inspections/viant-puerto-rico-inc/c2741209-2535-4cf2-857d-5eae2734df66)
- [FDA Inspection 1268767 - 2025-05-02](https://www.globalkeysolutions.net/records/fda_inspections/viant-puerto-rico-inc/e30a5e6e-9e43-4ac1-a116-275c01ff4388)

Company: https://www.globalkeysolutions.net/companies/viant-puerto-rico-inc/09c9fa1a-d7fb-4b1c-bf4e-54c448fd8255

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