FDA Warning Letter — Merete GmbH

Case 571091 — FEI 3002949614

The FDA took a Warning Letter action against Merete GmbH on Dec 31, 2018 (Berlin, Germany). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Merete GmbH
Date
Dec 31, 2018
Fiscal Year
2019
Product Type
Devices
Center
CDRH
Location
Berlin (Germany)