FDA Inspection
Stryker Medical Division of Stryker CorporationStryker Medical Division of Stryker Corporation – FDA Inspection, Sep 24, 2010
Record Details
This FDA Inspection record concerns Stryker Medical Division of Stryker Corporation, with an inspection on September 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 24, 2010
- Product Type
- Devices
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ID · adb590a9-b0b4-448e-acac-e65b4da497d7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 682480
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 803.50(a)(2)Individual Report of Malfunction
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Other FDA inspections of Stryker Medical Division of Stryker Corporation
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 15, 2024 | VAI | Detroit District Office | Compliance: Medical Devices |
| March 1, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 13, 2016 | Not classified | Detroit District Office | |
| June 26, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 15, 2009 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Stryker Medical Division of Stryker Corporation
- FDA Inspection 1255124 - 2024-11-15
- FDA Inspection 1003139 - 2017-03-01
- FDA Inspection 996318 - 2016-10-13
- FDA Inspection 791490 - 2012-06-26
- FDA Inspection 584103 - 2009-05-15
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