FDA Warning Letter — MEDDEV USA, INC.

Case 354319 — FEI 3009257101

The FDA took a Warning Letter action against MEDDEV USA, INC. on October 9, 2012 (Dallas, TX). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
MEDDEV USA, INC.
Date
October 9, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Dallas, TX (United States)