FDA Warning Letter — Spinalight, Inc.

Case 243494 — FEI 3006315109

The FDA took a Warning Letter action against Spinalight, Inc. on January 9, 2012 (Saint Petersburg, FL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Spinalight, Inc.
Date
January 9, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Saint Petersburg, FL (United States)