FDA Warning Letter — Talisman Limited

Case 98966 — FEI 3004585612

The FDA took a Warning Letter action against Talisman Limited on March 11, 2010 (Leesburg, VA). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Talisman Limited
Date
March 11, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Leesburg, VA (United States)