FDA Warning Letter — Mediagnost GmbH

Case 285197 — FEI 3003283395

The FDA took a Warning Letter action against Mediagnost GmbH on May 9, 2012 (Reutlingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Mediagnost GmbH
Date
May 9, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Reutlingen (Germany)