FDA Warning Letter — Octapharma AB

Case 179372 — FEI 3005559915

The FDA took a Warning Letter action against Octapharma AB on Apr 15, 2011 (Stockholm, Sweden). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action details

Facility
Octapharma AB
Date
Apr 15, 2011
Fiscal Year
2011
Product Type
Biologics
Center
CBER
Location
Stockholm (Sweden)

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