FDA Warning Letter — Medispec Ltd

Case 93664 — FEI 1000136413

The FDA took a Warning Letter action against Medispec Ltd on Mar 12, 2010 (Gaithersburg, MD). The action was issued by CDRH and concerns devices products.

Action Details

Facility
Medispec Ltd
Date
Mar 12, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Gaithersburg, MD (United States)