# FDA Inspection 631527 - Smith & Nephew - December 02, 2009

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew/4a6af14d-439a-412e-907e-f402c21e083f
Source feed: FDA_Inspections

> FDA Inspection 631527 for Smith & Nephew on December 02, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 631527
- Company Name: Smith & Nephew
- Inspection Date: 2009-12-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 631527 - 2009-12-02](https://www.keypedia.com/records/fda_inspections/smith-nephew/4fe508eb-4c9f-4275-a8a5-7e4efcd35702)

Company: https://www.keypedia.com/companies/smith-nephew/c7492e40-480d-4b8c-a53c-7fbabe8804fd

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