FDA Warning Letter — Spineology, Inc.

Case 128090 — FEI 3003179719

The FDA took a Warning Letter action against Spineology, Inc. on September 22, 2010 (Saint Paul, MN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Spineology, Inc.
Date
September 22, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Saint Paul, MN (United States)