# FDA Inspection 731758 - Braebon Medical Corp. - June 29, 2011

Source: https://www.keypedia.com/records/fda_inspections/braebon-medical-corp/4245af39-d301-46bb-b403-1fc1d7966bdd
Source feed: FDA_Inspections

> FDA Inspection 731758 for Braebon Medical Corp. on June 29, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 731758
- Company Name: Braebon Medical Corp.
- Inspection Date: 2011-06-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 931236 - 2015-06-23](https://www.keypedia.com/records/fda_inspections/braebon-medical-corp/8cea986e-a5ed-46eb-9f6c-fa690aaee186)
- [FDA Inspection 931236 - 2015-06-23](https://www.keypedia.com/records/fda_inspections/braebon-medical-corp/13a05959-c56f-4505-93d9-b41ab3643232)
- [FDA Inspection 731758 - 2011-06-29](https://www.keypedia.com/records/fda_inspections/braebon-medical-corp/674f1be7-d7e0-4d19-aabc-75c2a0e18c60)

Company: https://www.keypedia.com/companies/braebon-medical-corp/57665db2-034e-4ca5-82bb-dce3cf3968e7

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