FDA Inspection
Buxton Biomedical IncBuxton Biomedical Inc – FDA Inspection, Dec 22, 2011
Record Details
This FDA Inspection record concerns Buxton Biomedical Inc, with an inspection on December 22, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Buxton Biomedical Inc
- Inspection Date
- December 22, 2011
- Product Type
- Devices
View Company Profile
ID · 2635fd24-4134-4cc4-9385-c1947061c951
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 760596
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 803.17(b)(1)Info evaluated to determine if event was reportable
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Buxton Biomedical Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 21, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 27, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Buxton Biomedical Inc
- FDA Inspection 900734 - 2014-10-21
- FDA Inspection 599667 - 2009-07-27
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