FDA Warning Letter — Combo AG

Case 443070 — FEI 3004540983

The FDA took a Warning Letter action against Combo AG on January 12, 2015 (Lommiswil, Switzerland). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Combo AG
Date
January 12, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Lommiswil (Switzerland)