# FDA Inspection 815747 - Permobil AB - October 11, 2012

Source: https://www.keypedia.com/records/fda_inspections/permobil-ab/d31e5e1c-86f2-4c1e-b215-46d29b759954
Source feed: FDA_Inspections

> FDA Inspection 815747 for Permobil AB on October 11, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 815747
- Company Name: Permobil AB
- Inspection Date: 2012-10-11
- 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.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