FDA Inspection
Smith & Nephew Orthopaedics GmbHSmith & Nephew Orthopaedics GmbH – FDA Inspection, Jul 22, 2010
Record Details
This FDA Inspection record concerns Smith & Nephew Orthopaedics GmbH, with an inspection on July 22, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 22, 2010
- Product Type
- Devices
View Company Profile
ID · 2be7a615-b2c7-4abf-a68b-ef6790a24bbc
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 681881
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
Other FDA inspections of Smith & Nephew Orthopaedics GmbH
6| Date | Classification | Office | Project area |
|---|---|---|---|
| January 12, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 8, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| April 6, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 7, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 22, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Smith & Nephew Orthopaedics GmbH
- FDA Inspection 1199981 - 2023-01-12
- FDA Inspection 1045278 - 2018-02-08
- FDA Inspection 1022654 - 2017-04-06
- FDA Inspection 928966 - 2015-05-07
- FDA Inspection 823996 - 2013-02-22
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