# FDA Inspection 646909 - Arcoma AB - January 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/arcoma-ab/036502eb-ce5e-4825-9730-48fbd2a19310
Source feed: FDA_Inspections

> FDA Inspection 646909 for Arcoma AB on January 19, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 646909
- Company Name: Arcoma AB
- Inspection Date: 2010-01-19
- 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 839779 - 2013-06-27](https://www.keypedia.com/records/fda_inspections/arcoma-ab/9fa68813-f027-43b2-a67f-070b6f5c1321)

Company: https://www.keypedia.com/companies/arcoma-ab/80d7c04d-2d1a-4563-b65f-6cedbb225495

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