# FDA Inspection 900734 - Buxton Biomedical Inc - October 21, 2014

Source: https://www.keypedia.com/records/fda_inspections/buxton-biomedical-inc/f505016b-336a-4088-a8ce-9179423a29a3
Source feed: FDA_Inspections

> FDA Inspection 900734 for Buxton Biomedical Inc on October 21, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900734
- Company Name: Buxton Biomedical Inc
- Inspection Date: 2014-10-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 760596 - 2011-12-22](https://www.keypedia.com/records/fda_inspections/buxton-biomedical-inc/2635fd24-4134-4cc4-9385-c1947061c951)
- [FDA Inspection 760596 - 2011-12-22](https://www.keypedia.com/records/fda_inspections/buxton-biomedical-inc/12497b6a-a417-4182-a33d-bf18740d5d90)
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- [FDA Inspection 599667 - 2009-07-27](https://www.keypedia.com/records/fda_inspections/buxton-biomedical-inc/56f28e9f-a190-41af-850b-f0340daf62cb)

Company: https://www.keypedia.com/companies/buxton-biomedical-inc/d0fd2abd-522a-4ba1-bed3-94ca515dafcf

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7