# FDA Inspection 843550 - Bioconnect, Div of RF Industries - July 24, 2013

Source: https://www.keypedia.com/records/fda_inspections/bioconnect-div-of-rf-industries/4f4d30bd-cef0-445c-8cb9-435a4d2f4f3f
Source feed: FDA_Inspections

> FDA Inspection 843550 for Bioconnect, Div of RF Industries on July 24, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 843550
- Company Name: Bioconnect, Div of RF Industries
- Inspection Date: 2013-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 843550 - 2013-07-24](https://www.keypedia.com/records/fda_inspections/bioconnect-div-of-rf-industries/b38585d4-75ce-448b-9999-9c336d6df55a)

Company: https://www.keypedia.com/companies/bioconnect-div-of-rf-industries/b644f61d-022f-4703-8937-a06167990145

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