FDA Inspection
Permobil IncPermobil Inc – FDA Inspection, Jan 11, 2018
Record Details
This FDA Inspection record concerns Permobil Inc, with an inspection on January 11, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · faf1f571-a19e-4997-90fd-74f91f986de8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1037821
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, 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 |
| August 17, 2021 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: 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 1149139 - 2021-08-17
- FDA Inspection 927931 - 2015-05-28
- FDA Inspection 768863 - 2012-02-16
- FDA Inspection 599948 - 2009-07-21
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