# FDA Inspection 959726 - Permobil AB - February 12, 2016

Source: https://www.keypedia.com/records/fda_inspections/permobil-ab/b7e4fdb8-df12-4a1a-bcd2-4d654a26b7ba
Source feed: FDA_Inspections

> FDA Inspection 959726 for Permobil AB on February 12, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 959726
- Company Name: Permobil AB
- Inspection Date: 2016-02-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 959726 - 2016-02-12](https://www.keypedia.com/records/fda_inspections/permobil-ab/8d59526e-46aa-415f-81be-9c3ef0d6c4ed)
- [FDA Inspection 815747 - 2012-10-11](https://www.keypedia.com/records/fda_inspections/permobil-ab/d31e5e1c-86f2-4c1e-b215-46d29b759954)
- [FDA Inspection 815747 - 2012-10-11](https://www.keypedia.com/records/fda_inspections/permobil-ab/3d20c7f6-a290-4570-9704-35aee0ff7f3e)

Company: https://www.keypedia.com/companies/permobil-ab/55abff39-4f04-47a6-81c7-d6314891a9f5

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