FDA Warning Letter — SpineFrontier, Inc.

Case 334199 — FEI 3005977257

The FDA took a Warning Letter action against SpineFrontier, Inc. on August 8, 2012 (Burlington, MA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
SpineFrontier, Inc.
Date
August 8, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Burlington, MA (United States)