# FDA Inspection 612366 - Byron Medical, Inc - September 11, 2009

Source: https://www.keypedia.com/records/fda_inspections/byron-medical-inc/a98be176-9ac3-4557-a711-d5467c21e661
Source feed: FDA_Inspections

> FDA Inspection 612366 for Byron Medical, Inc on September 11, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 612366
- Company Name: Byron Medical, Inc
- Inspection Date: 2009-09-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 612366 - 2009-09-11](https://www.keypedia.com/records/fda_inspections/byron-medical-inc/8c51c5c9-48a8-4908-a0a5-0a1792acc97c)

Company: https://www.keypedia.com/companies/byron-medical-inc/11d43472-d836-4611-bc86-2fd72025e89a

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