FDA Warning Letter — Vibracare Gmbh

Case 450437 — FEI 3010275727

The FDA took a Warning Letter action against Vibracare Gmbh on April 17, 2015 (Bremen, Germany). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Vibracare Gmbh
Date
April 17, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Bremen (Germany)