# FDA Inspection 1261947 - ALPHA LASER Gmbh - September 12, 2024

Source: https://www.keypedia.com/records/fda_inspections/alpha-laser-gmbh/b2689d73-a029-40a9-9450-0e069412027c
Source feed: FDA_Inspections

> FDA Inspection 1261947 for ALPHA LASER Gmbh on September 12, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1261947
- Company Name: ALPHA LASER Gmbh
- Inspection Date: 2024-09-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1261947 - 2024-09-12](https://www.keypedia.com/records/fda_inspections/alpha-laser-gmbh/eeb7794c-0919-441b-bbc1-1a13fb43d9ec)

Company: https://www.keypedia.com/companies/alpha-laser-gmbh/ac7bd144-b8dd-4ea4-9840-3f89cc4cab12

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