FDA Warning Letter — Howard Instruments Inc

Case 50101 — FEI 1039865

The FDA took a Warning Letter action against Howard Instruments Inc on May 12, 2009 (Tuscaloosa, AL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Howard Instruments Inc
Date
May 12, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Tuscaloosa, AL (United States)