# FDA Inspection 830218 - Q-Med AB - April 25, 2013

Source: https://www.keypedia.com/records/fda_inspections/q-med-ab/93417339-81d7-4a8a-9f2e-03f0aeb74df0
Source feed: FDA_Inspections

> FDA Inspection 830218 for Q-Med AB on April 25, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830218
- Company Name: Q-Med AB
- Inspection Date: 2013-04-25
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 830218 - 2013-04-25](https://www.keypedia.com/records/fda_inspections/q-med-ab/9601ed9d-031b-44b8-8481-3cb1cc463c0c)
- [FDA Inspection 567005 - 2009-01-29](https://www.keypedia.com/records/fda_inspections/q-med-ab/f2f32c92-8001-466d-840f-46135804dc8f)
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Company: https://www.keypedia.com/companies/q-med-ab/e15afce0-b37c-4e64-8da1-15f21db64c47

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