# FDA Inspection 921654 - Q-Med AB - February 13, 2015

Source: https://www.keypedia.com/records/fda_inspections/q-med-ab/278d0e12-4196-4c92-8311-7e6e438f848c
Source feed: FDA_Inspections

> FDA inspection 921654 of Q-Med AB, February 13, 2015. Classification: No Action Indicated (NAI). 7 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 921654
- Company Name: Q-Med AB
- Inspection Date: 2015-02-13
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1313816 - 2026-03-27](https://www.keypedia.com/records/fda_inspections/q-med-ab/21b37783-5d36-4ad4-8fd2-8656ff3b6b52)
- FDA Inspection 1199979 - 2023-01-19
- FDA Inspection 1048550 - 2018-03-29
- [FDA Inspection 1025913 - 2017-08-24](https://www.keypedia.com/records/fda_inspections/q-med-ab/ebec262d-2d9e-4346-9d98-31e8bf2afa18)
- [FDA Inspection 789285 - 2012-06-21](https://www.keypedia.com/records/fda_inspections/q-med-ab/fb513c8e-77af-4151-9a93-b3c6599e7159)

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

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