# FDA Inspection 1048550 - Q-Med AB - March 29, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/q-med-ab/f80e38bd-954a-4805-baf2-3f08c7c5ad90/
Source feed: FDA_Inspections

> FDA Inspection 1048550 for Q-Med AB on March 29, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048550
- Company Name: Q-Med AB
- Inspection Date: 2018-03-29
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/q-med-ab/032a27fc-d1ee-4ed3-98da-38090c026849

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