# FDA Inspection 839779 - Arcoma AB - June 27, 2013

Source: https://www.keypedia.com/records/fda_inspections/arcoma-ab/9fa68813-f027-43b2-a67f-070b6f5c1321
Source feed: FDA_Inspections

> FDA Inspection 839779 for Arcoma AB on June 27, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839779
- Company Name: Arcoma AB
- Inspection Date: 2013-06-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 646909 - 2010-01-19](https://www.keypedia.com/records/fda_inspections/arcoma-ab/036502eb-ce5e-4825-9730-48fbd2a19310)

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