# FDA Inspection 939280 - Smith & Nephew Medical, Ltd. - July 09, 2015

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-medical-ltd/99b3e71e-677e-429c-ae3d-cef5c22d1743
Source feed: FDA_Inspections

> FDA Inspection 939280 for Smith & Nephew Medical, Ltd. on July 09, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 939280
- Company Name: Smith & Nephew Medical, Ltd.
- Inspection Date: 2015-07-09
- 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 939280 - 2015-07-09](https://www.keypedia.com/records/fda_inspections/smith-nephew-medical-ltd/935e7f09-6535-4cb7-9973-c4a09cfbeab3)

Company: https://www.keypedia.com/companies/smith-nephew-medical-ltd/9d1b9dd6-1c47-4913-b4bc-909ee40d7eff

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