# Smith & Nephew Orthopaedics GmbH - Inspection Records

Source: https://www.keypedia.com/companies/smith-nephew-orthopaedics-gmbh/65d3d2bd-0c5f-486d-ab89-d6c131368645

> Inspection records and compliance data for Smith & Nephew Orthopaedics GmbH in Tuttlingen, None. Access full analysis and detailed observations.

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## Details

- Name: Smith & Nephew Orthopaedics GmbH
- FEI Number: 3002465897
- City: Tuttlingen
- State: None
- Country Name: Germany
- Address Line 1: Alemannenstr. 14
- Zip Code: None

## Related Documents

- [FDA Inspection 1199981 - Smith & Nephew Orthopaedics GmbH - 2023-01-12](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/023d4417-dd73-4d64-a824-2188b3d03d20) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 12, 2023
- [FDA Inspection 1045278 - Smith & Nephew Orthopaedics GmbH - 2018-02-08](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/f1b39e5e-fdf7-41c3-a3b9-8030cb0c95cf) — classification: No Action Indicated (NAI), source: FDA, date: February 8, 2018
- [FDA Inspection 1022654 - Smith & Nephew Orthopaedics GmbH - 2017-04-06](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/5e2a1288-b82e-4ce1-a2fa-f61a5bda1383) — classification: No Action Indicated (NAI), source: FDA, date: April 6, 2017
- [FDA Inspection 928966 - Smith & Nephew Orthopaedics GmbH - 2015-05-07](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/53352ad7-fca9-42ce-a058-2846736c073e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2015
- [FDA Inspection 928966 - Smith & Nephew Orthopaedics GmbH - 2015-05-07](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/f147a54a-fbdf-4cd0-934a-792ceacaf0df) — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2015
- [FDA Inspection 823996 - Smith & Nephew Orthopaedics GmbH - 2013-02-22](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/8806faca-9fd7-45d3-a228-71e8e7ef3a76) — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2013
- [FDA Inspection 823996 - Smith & Nephew Orthopaedics GmbH - 2013-02-22](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/19a045de-6ca0-4a4c-9fce-bdbb49c2f040) — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2013
- [FDA Inspection 681881 - Smith & Nephew Orthopaedics GmbH - 2010-07-22](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/2be7a615-b2c7-4abf-a68b-ef6790a24bbc) — classification: Official Action Indicated (OAI), source: FDA, date: July 22, 2010
- [FDA Inspection 555056 - Smith & Nephew Orthopaedics GmbH - 2008-11-13](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/e292d5d0-ce2f-4405-bdaa-e497d3ebefa2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 13, 2008
- [FDA Inspection 555056 - Smith & Nephew Orthopaedics GmbH - 2008-11-13](https://www.keypedia.com/records/fda_inspections/smith-nephew-orthopaedics-gmbh/68671554-60cb-47d9-8b17-fca6feb047e6) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2008

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