# FDA Inspection 922173 - Smith & Nephew Orthopaedics AG - March 05, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/smith-nephew-orthopaedics-ag/2fc2e2c5-37b5-4118-b62e-e8495155f083
Source feed: FDA_Inspections

> FDA Inspection 922173 for Smith & Nephew Orthopaedics AG on March 05, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 922173
- Company Name: Smith & Nephew Orthopaedics AG
- Inspection Date: 2015-03-05
- 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 922173 - 2015-03-05](https://www.globalkeysolutions.net/records/fda_inspections/smith-nephew-orthopaedics-ag/bb5cd34e-dec3-4d48-a7d0-20d4310ae7ad)
- [FDA Inspection 620825 - 2009-09-10](https://www.globalkeysolutions.net/records/fda_inspections/smith-nephew-orthopaedics-ag/fa637e42-8cc1-482b-8f3f-3ef60ad3d540)

Company: https://www.globalkeysolutions.net/companies/smith-nephew-orthopaedics-ag/aa971d32-383b-4cc1-9886-0599fd95525b

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