FDA Warning Letter — Meditech KFT

Case 314858 — FEI 3003764019

The FDA took a Warning Letter action against Meditech KFT on July 18, 2012 (Budapest, Hungary). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Meditech KFT
Date
July 18, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Budapest (Hungary)