FDA Inspection
Permobil IncPermobil Inc – FDA Inspection, Feb 16, 2012
Record Details
This FDA Inspection record concerns Permobil Inc, with an inspection on February 16, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Permobil Inc
- Inspection Date
- February 16, 2012
- Product Type
- Devices
View Company Profile
ID · c0ff0209-3810-4682-b414-1036ccdfa528
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 768863
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.184DHR content
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 |
| January 11, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 28, 2015 | NAI | 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 1037821 - 2018-01-11
- FDA Inspection 927931 - 2015-05-28
- FDA Inspection 599948 - 2009-07-21
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