FDA Warning Letter — UltraRad Corporation

Case 61563 — FEI 3000149131

The FDA took a Warning Letter action against UltraRad Corporation on May 29, 2009 (Voorhees, NJ). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
UltraRad Corporation
Date
May 29, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Voorhees, NJ (United States)