FDA Warning Letter — Curasan AG, Frankfurt Facility

Case 534581 — FEI 3004847139

The FDA took a Warning Letter action against Curasan AG, Frankfurt Facility on August 23, 2017 (Frankfurt Am Main, Germany). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Curasan AG, Frankfurt Facility
Date
August 23, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Frankfurt Am Main (Germany)