# FDA Inspection 1022917 - Silver Ring Splint Company - July 07, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/silver-ring-splint-company/fb29c384-3b5d-4ad2-87e7-3f173eb274fe/
Source feed: FDA_Inspections

> FDA Inspection 1022917 for Silver Ring Splint Company on July 07, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022917
- Company Name: Silver Ring Splint Company
- Inspection Date: 2017-07-07
- 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 1022917 - 2017-07-07](https://www.globalkeysolutions.net/api/records/fda_inspections/silver-ring-splint-company/a62203b4-815e-4bf4-ad3b-585adb3345b4/)

Company: https://www.globalkeysolutions.net/companies/silver-ring-splint-company/fcd6b0f5-906d-4a04-987a-f6a0c93da85c

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