# FDA Inspection 935470 - Smith & Nephew Inc - July 23, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/smith-nephew-inc/fc7769d2-a94e-4141-bdc6-19f3c733f0ac/
Source feed: FDA_Inspections

> FDA Inspection 935470 for Smith & Nephew Inc on July 23, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935470
- Company Name: Smith & Nephew Inc
- Inspection Date: 2015-07-23
- 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 935470 - 2015-07-23](https://www.globalkeysolutions.net/api/records/fda_inspections/smith-nephew-inc/cc956a5d-f3b0-437d-b678-1ccf0db197d3/)
- [FDA Inspection 700982 - 2010-12-02](https://www.globalkeysolutions.net/api/records/fda_inspections/smith-nephew-inc/7645a417-dded-4d1c-b15c-518d17372251/)
- [FDA Inspection 606405 - 2009-08-19](https://www.globalkeysolutions.net/api/records/fda_inspections/smith-nephew-inc/0af3e81c-2f2d-4fab-ae2d-456510a91105/)

Company: https://www.globalkeysolutions.net/companies/smith-nephew-inc/192f578a-af69-4ca8-a42e-6567c1b5fee9

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