FDA Warning Letter — Cenova AB

Case 158492 — FEI 3005216725

The FDA took a Warning Letter action against Cenova AB on Feb 25, 2011 (Mjolby, Sweden). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action details

Facility
Cenova AB
Date
Feb 25, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Mjolby (Sweden)

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