# FDA Inspection 1015137 - Smith & Nephew, Inc. - May 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/52e2652a-270d-44f5-9f42-b5f89ac3263f
Source feed: FDA_Inspections

> FDA Inspection 1015137 for Smith & Nephew, Inc. on May 25, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015137
- Company Name: Smith & Nephew, Inc.
- Inspection Date: 2017-05-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 960574 - 2015-12-08](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/791e03db-6cce-48d8-a22c-c05906e33dd0)
- [FDA Inspection 740641 - 2011-08-15](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/222e3ce1-d872-459f-90fc-18018f5755df)

Company: https://www.keypedia.com/companies/smith-nephew-inc/000fa36f-a97a-49b7-8a63-1a5c135e6f31

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