# FDA Inspection 1269851 - Cenova AB - May 08, 2025

Source: https://www.keypedia.com/records/fda_inspections/cenova-ab/2c78650a-d265-4080-886a-0c2d2df647d7
Source feed: FDA_Inspections

> FDA Inspection 1269851 for Cenova AB on May 08, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1269851
- Company Name: Cenova AB
- Inspection Date: 2025-05-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1269851 - 2025-05-08](https://www.keypedia.com/records/fda_inspections/cenova-ab/c89966f5-1e57-4482-a861-1e2590c71365)
- [FDA Inspection 1194250 - 2022-11-18](https://www.keypedia.com/records/fda_inspections/cenova-ab/ff22f9b3-9333-41c7-80f8-b4723082182b)

Company: https://www.keypedia.com/companies/cenova-ab/d4ee8c27-2f15-46f7-9265-d7a5afacc0f4

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