FDA Inspection
Buxton Biomedical IncBuxton Biomedical Inc – FDA Inspection, Jul 27, 2009
Record Details
This FDA Inspection record concerns Buxton Biomedical Inc, with an inspection on July 27, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Buxton Biomedical Inc
- Inspection Date
- July 27, 2009
- Product Type
- Devices
View Company Profile
ID · 56f28e9f-a190-41af-850b-f0340daf62cb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 599667
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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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 |
| December 22, 2011 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Buxton Biomedical Inc
- FDA Inspection 900734 - 2014-10-21
- FDA Inspection 760596 - 2011-12-22
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