# FDA Inspection 1037821 - Permobil Inc - January 11, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/permobil-inc/faf1f571-a19e-4997-90fd-74f91f986de8/
Source feed: FDA_Inspections

> FDA Inspection 1037821 for Permobil Inc on January 11, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037821
- Company Name: Permobil Inc
- Inspection Date: 2018-01-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/permobil-inc/61d4e282-3d2e-4264-a233-860e885f4716

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