FDA Inspection
Vertebral Technologies, Inc.Vertebral Technologies, Inc. – FDA Inspection, Nov 16, 2016
Record Details
This FDA Inspection record concerns Vertebral Technologies, Inc., with an inspection on November 16, 2016, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 91b487da-9ff3-434c-bdef-4c7428d5be70
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 994689
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 806.10(a)(2)Report of violation of the Act (see 803.52(e)(9))
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Vertebral Technologies, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 2, 2015 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 16, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 12, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Vertebral Technologies, Inc.
- FDA Inspection 912320 - 2015-02-02
- FDA Inspection 776625 - 2012-04-16
- FDA Inspection 588231 - 2009-06-12
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.