FDA Warning Letter — Instrumed GmbH

Case 415984 — FEI 3007290840

The FDA took a Warning Letter action against Instrumed GmbH on March 28, 2014 (Tuttlingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Instrumed GmbH
Date
March 28, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Tuttlingen (Germany)