# FDA Inspection 1307052 - Altor Safety - March 12, 2026

Source: https://www.keypedia.com/records/fda_inspections/altor-safety/0a87ed5b-74d3-4da8-956b-26453c652d34
Source feed: FDA_Inspections

> FDA Inspection 1307052 for Altor Safety on March 12, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1307052
- Company Name: Altor Safety
- Inspection Date: 2026-03-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1307052 - 2026-03-12](https://www.keypedia.com/records/fda_inspections/altor-safety/530c9835-9a49-426e-97a9-a9a83eebdc6b)
- [FDA Inspection 1307052 - 2026-03-12](https://www.keypedia.com/records/fda_inspections/altor-safety/052a4f4d-5640-4172-ad7d-18e8d2ea2d1c)
- [FDA Inspection 1307052 - 2026-03-12](https://www.keypedia.com/records/fda_inspections/altor-safety/c6d42fc6-5363-4bed-988b-2e9f9ffb9690)

Company: https://www.keypedia.com/companies/altor-safety/0f2af77b-17a2-40d4-a0fe-be65b71ed6cc

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