FDA Inspection
VertiFlex, Inc.VertiFlex, Inc. – FDA Inspection, Feb 11, 2010
Record Details
This FDA Inspection record concerns VertiFlex, Inc., with an inspection on February 11, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- VertiFlex, Inc.
- Inspection Date
- February 11, 2010
- Product Type
- Devices
View Company Profile
ID · 96b6012b-af16-4126-b274-1b7d383f1618
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 647468
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of VertiFlex, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 19, 2016 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| July 25, 2014 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| May 16, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 7, 2008 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for VertiFlex, Inc.
- FDA Inspection 993550 - 2016-07-19
- FDA Inspection 888763 - 2014-07-25
- FDA Inspection 881232 - 2014-05-16
- FDA Inspection 541038 - 2008-10-07
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