FDA Inspection
Permobil IncPermobil Inc – FDA Inspection, Aug 17, 2021
Record Details
This FDA Inspection record concerns Permobil Inc, with an inspection on August 17, 2021, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Permobil Inc
- Inspection Date
- August 17, 2021
- Product Type
- Devices
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ID · 9ee203be-042f-41b3-ad3d-a0662cd7c003
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1149139
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Permobil Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 16, 2026 | Not classified | New Orleans District Office | Compliance: Devices |
| January 11, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 28, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 16, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 21, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Permobil Inc
- FDA Inspection 1299994 - 2026-04-16
- FDA Inspection 1037821 - 2018-01-11
- FDA Inspection 927931 - 2015-05-28
- FDA Inspection 768863 - 2012-02-16
- FDA Inspection 599948 - 2009-07-21
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