# FDA Inspection 927931 - Permobil Inc - May 28, 2015

Source: https://www.keypedia.com/records/fda_inspections/permobil-inc/30a0c356-e890-485f-a8a2-9e0b8c61a732
Source feed: FDA_Inspections

> FDA Inspection 927931 for Permobil Inc on May 28, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 927931
- Company Name: Permobil Inc
- Inspection Date: 2015-05-28
- 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-inc/61d4e282-3d2e-4264-a233-860e885f4716

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