# Arcoma AB – FDA Inspection, Jan 19, 2010

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

> FDA inspection 646909 of Arcoma AB, January 19, 2010. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 1020. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 839779 - 2013-06-27

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