FDA Inspection 802513 — Fresenius Kabi AB

Fresenius Kabi AB — FEI 3002631703

The FDA completed an inspection of Fresenius Kabi AB on Sep 25, 2012 in Uppsala. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 25, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Uppsala (Sweden)

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