# FDA Inspection 936431 - Renfro Corporation - June 16, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/renfro-corporation/f71fadc4-d198-4498-afa2-31c42092abc0/
Source feed: FDA_Inspections

> FDA Inspection 936431 for Renfro Corporation on June 16, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 936431
- Company Name: Renfro Corporation
- Inspection Date: 2015-06-16
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 936431 - 2015-06-16](https://www.globalkeysolutions.net/api/records/fda_inspections/renfro-corporation/66f27909-d349-40c8-9af2-17632b835259/)

Company: https://www.globalkeysolutions.net/companies/renfro-corporation/d5f9b88a-a3a8-47fc-bd35-776f2ab33a5b

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