# FDA Inspection 1215912 - INTRAVU INC - July 07, 2023

Source: https://www.keypedia.com/records/fda_inspections/intravu-inc/8d5ec0ad-41cd-43d7-ba1d-55eb6592dc6b
Source feed: FDA_Inspections

> FDA Inspection 1215912 for INTRAVU INC on July 07, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1215912
- Company Name: INTRAVU INC
- Inspection Date: 2023-07-07
- 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 1215912 - 2023-07-07](https://www.keypedia.com/records/fda_inspections/intravu-inc/776d5919-0c23-4e81-a24f-451d8e30121c)

Company: https://www.keypedia.com/companies/intravu-inc/bb00f1a3-6f14-4244-94b6-07295e2fdfcc

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