# FDA Inspection 893811 - Unfors RaySafe AB - September 03, 2014

Source: https://www.keypedia.com/records/fda_inspections/unfors-raysafe-ab/48acf77b-98be-4858-930a-da699e9d4504
Source feed: FDA_Inspections

> FDA Inspection 893811 for Unfors RaySafe AB on September 03, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 893811
- Company Name: Unfors RaySafe AB
- Inspection Date: 2014-09-03
- 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 893811 - 2014-09-03](https://www.keypedia.com/records/fda_inspections/unfors-raysafe-ab/58ec42ac-628c-4999-a1b7-72c7f51ea617)

Company: https://www.keypedia.com/companies/unfors-raysafe-ab/bf593c9b-ca6c-4d0d-8a88-20c38209361d

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