FDA Warning Letter — Alphatec Spine, Inc.

Case 100065 — FEI 2027467

The FDA took a Warning Letter action against Alphatec Spine, Inc. on June 21, 2010 (Carlsbad, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Alphatec Spine, Inc.
Date
June 21, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Carlsbad, CA (United States)