# FDA Inspection 1034176 - Renfro Charleston LLC - November 28, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/renfro-charleston-llc/843f8b98-38cb-4500-b291-ce7f9a57d6d2
Source feed: FDA_Inspections

> FDA Inspection 1034176 for Renfro Charleston LLC on November 28, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034176
- Company Name: Renfro Charleston LLC
- Inspection Date: 2017-11-28
- 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 1034176 - 2017-11-28](https://www.globalkeysolutions.net/records/fda_inspections/renfro-charleston-llc/b4d40f81-1258-49bb-be0b-427be16c1ccc)

Company: https://www.globalkeysolutions.net/companies/renfro-charleston-llc/7907a7dd-7d53-44ea-825f-aa9ba5490ddf

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