# FDA Inspection 732318 - VivaRay Inc. - June 30, 2011

Source: https://www.keypedia.com/records/fda_inspections/vivaray-inc/981577b5-2079-46fe-94a6-1e89ae2f8d17
Source feed: FDA_Inspections

> FDA Inspection 732318 for VivaRay Inc. on June 30, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 732318
- Company Name: VivaRay Inc.
- Inspection Date: 2011-06-30
- 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 732318 - 2011-06-30](https://www.keypedia.com/records/fda_inspections/vivaray-inc/e4df50d6-3ff9-4f40-83a3-eee204bfd52c)

Company: https://www.keypedia.com/companies/vivaray-inc/c3e133ad-76ad-4a8d-aed4-c58cde3dd837

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