FDA Warning Letter — MKL DIAGNOSTICS AB

Case 430843 — FEI 3009335508

The FDA took a Warning Letter action against MKL DIAGNOSTICS AB on July 29, 2014 (Sollentuna, Sweden). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
MKL DIAGNOSTICS AB
Date
July 29, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Sollentuna (Sweden)