# FDA Inspection 884305 - Smith & Nephew - June 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew/05e0e477-8469-4108-beea-19a2e84d6868
Source feed: FDA_Inspections

> FDA Inspection 884305 for Smith & Nephew on June 24, 2014. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 884305
- Company Name: Smith & Nephew
- Inspection Date: 2014-06-24
- 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 1042563 - 2018-01-30](https://www.keypedia.com/records/fda_inspections/smith-nephew/b3e275d8-a453-4ed7-a251-1112633fb489)
- [FDA Inspection 983397 - 2016-08-18](https://www.keypedia.com/records/fda_inspections/smith-nephew/266cea28-d095-49e5-a66d-0ca60437eef5)
- [FDA Inspection 884305 - 2014-06-24](https://www.keypedia.com/records/fda_inspections/smith-nephew/71d04e40-fc01-4ba0-9690-8f699d23a454)

Company: https://www.keypedia.com/companies/smith-nephew/05e7b474-8abe-43ec-ae37-3909b770d363

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