FDA Warning Letter — Sopro Comeg Gmbh

Case 432749 — FEI 3005840432

The FDA took a Warning Letter action against Sopro Comeg Gmbh on Feb 23, 2015 (Tuttlingen, Germany). The action was issued by CDRH and concerns devices products.

Action Details

Facility
Sopro Comeg Gmbh
Date
Feb 23, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Tuttlingen (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.