# FDA Inspection 1149139 - Permobil Inc - August 17, 2021

Source: https://www.keypedia.com/records/fda_inspections/permobil-inc/3eefc70c-d2d4-47e6-8fea-5e3825c1a1be
Source feed: FDA_Inspections

> FDA Inspection 1149139 for Permobil Inc on August 17, 2021. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1149139
- Company Name: Permobil Inc
- Inspection Date: 2021-08-17
- 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.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