FDA Warning Letter — Syntron Bioresearch Inc

Case 95206 — FEI 2025760

The FDA took a Warning Letter action against Syntron Bioresearch Inc on May 24, 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
Syntron Bioresearch Inc
Date
May 24, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Carlsbad, CA (United States)