FDA Warning Letter — M Dialysis AB

Case 554169 — FEI 3003733874

The FDA took a Warning Letter action against M Dialysis AB on Jun 14, 2018 (Stockholm, Sweden). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
M Dialysis AB
Date
Jun 14, 2018
Fiscal Year
2018
Product Type
Devices
Center
CDRH
Location
Stockholm (Sweden)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.