# FDA Inspection 942195 - Orifice Medical AB - September 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/orifice-medical-ab/28e85ce9-444f-418c-a809-a7bb133f4b39
Source feed: FDA_Inspections

> FDA Inspection 942195 for Orifice Medical AB on September 17, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 942195
- Company Name: Orifice Medical AB
- Inspection Date: 2015-09-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 942195 - 2015-09-17](https://www.keypedia.com/records/fda_inspections/orifice-medical-ab/1159c5d1-03e7-4694-bbf5-44eff499a8fa)
- [FDA Inspection 642624 - 2009-11-23](https://www.keypedia.com/records/fda_inspections/orifice-medical-ab/28e4c76b-394a-4cde-adff-f598fb967612)

Company: https://www.keypedia.com/companies/orifice-medical-ab/a275d03f-b0fc-4f85-a8ad-3df984afda3c

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