# FDA Inspection 1225464 - CATHVISION APS - November 30, 2023

Source: https://www.keypedia.com/records/fda_inspections/cathvision-aps/cce118c4-b10e-4447-b064-6d7b51fa4c76
Source feed: FDA_Inspections

> FDA Inspection 1225464 for CATHVISION APS on November 30, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1225464
- Company Name: CATHVISION APS
- Inspection Date: 2023-11-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1225464 - 2023-11-30](https://www.keypedia.com/records/fda_inspections/cathvision-aps/5699de32-add6-4626-9d28-09132d63fa33)

Company: https://www.keypedia.com/companies/cathvision-aps/22223b75-ad37-48dc-9e5a-27503716a76a

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