FDA Inspection
SPINEART SASPINEART SA – FDA Inspection, Sep 10, 2013
Record Details
This FDA Inspection record concerns SPINEART SA, with an inspection on September 10, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- SPINEART SA
- Inspection Date
- September 10, 2013
- Product Type
- Devices
View Company Profile
ID · 1abde849-42ef-4a52-a5ec-0f1aa31d1b8c
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 852552
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of SPINEART SA
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 22, 2019 | Not classified | Office of Inspections and Investigations | |
| December 8, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for SPINEART SA
- FDA Inspection 1096341 - 2019-05-22
- FDA Inspection 996791 - 2016-12-08
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