FDA Inspection
Stryker CommunicationsStryker Communications – FDA Inspection, Mar 2, 2012
Record Details
This FDA Inspection record concerns Stryker Communications, with an inspection on March 2, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Stryker Communications
- Inspection Date
- March 2, 2012
- Product Type
- Devices
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ID · cf91695b-cb00-4fdc-b358-69cbb5d22563
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 770973
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 820.50(a)(2)Supplier oversight
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Other FDA inspections of Stryker Communications
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 25, 2017 | Not classified | Dallas District Office | |
| March 3, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 13, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 20, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 26, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Stryker Communications
- FDA Inspection 1029472 - 2017-05-25
- FDA Inspection 964567 - 2016-03-03
- FDA Inspection 806785 - 2012-11-13
- FDA Inspection 596865 - 2009-07-20
- FDA Inspection 556605 - 2009-01-26
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