FDA Inspection
DePuy Spine, Inc.DePuy Spine, Inc. – FDA Inspection, Apr 28, 2009
Record Details
This FDA Inspection record concerns DePuy Spine, Inc., with an inspection on April 28, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- DePuy Spine, Inc.
- Inspection Date
- April 28, 2009
- Product Type
- Devices
View Company Profile
ID · c37076db-4c2b-4515-a028-a3c9a414103e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 580522
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.70(a)Production processes
Full citation text and observation details available on the Dashboard.
Other FDA inspections of DePuy Spine, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| April 18, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 16, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 11, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 10, 2012 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| April 21, 2009 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for DePuy Spine, Inc.
- FDA Inspection 1090256 - 2019-04-18
- FDA Inspection 1021012 - 2017-06-16
- FDA Inspection 787390 - 2012-06-11
- FDA Inspection 767079 - 2012-02-10
- FDA Inspection 577762 - 2009-04-21
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