# FDA Inspection 681573 - Smith & Nephew, Inc. - September 13, 2010

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/9debbdba-6c91-4ddf-aaa9-c8a6d868e351
Source feed: FDA_Inspections

> FDA Inspection 681573 for Smith & Nephew, Inc. on September 13, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 681573
- Company Name: Smith & Nephew, Inc.
- Inspection Date: 2010-09-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1022775 - 2017-07-24](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/b4402eeb-414b-4543-b898-6d4a7e1264bc)

Company: https://www.keypedia.com/companies/smith-nephew-inc/a000a45c-a36d-44e0-a6ec-e1a212e37d61

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