# Permobil Inc – FDA Inspection, Jan 11, 2018

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

> FDA inspection 1037821 of Permobil Inc, January 11, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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## Related Officers

- [Mary A. Millner](https://www.keypedia.com/people/mary-a-millner/bd8911cf-849d-41d2-ae12-dd4bad66e798)

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