FDA Inspection
Zimmer Spine, Inc.Zimmer Spine, Inc. – FDA Inspection, Nov 6, 2009
Record Details
This FDA Inspection record concerns Zimmer Spine, Inc., with an inspection on November 6, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Zimmer Spine, Inc.
- Inspection Date
- November 6, 2009
- Product Type
- Devices
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ID · fca1ff08-2b86-4d9f-8984-4c23957dce29
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 630672
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 806.10(b)Time to report - 10 days
- 21 CFR 820.198(a)(1)Uniform and timely processing
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Other FDA inspections of Zimmer Spine, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 3, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Zimmer Spine, Inc.
- FDA Inspection 826674 - 2013-04-03
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