FDA Warning Letter — Vertebral Technologies, Inc.

Case 453675 — FEI 3007617183

The FDA took a Warning Letter action against Vertebral Technologies, Inc. on September 4, 2015 (Santa Clara, CA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Vertebral Technologies, Inc.
Date
September 4, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Santa Clara, CA (United States)