FDA Warning Letter — WEBER MEDICAL GMBH

Case 394666 — FEI 3007165178

The FDA took a Warning Letter action against WEBER MEDICAL GMBH on May 2, 2013 (Lauenforde, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
WEBER MEDICAL GMBH
Date
May 2, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Lauenforde (Germany)