FDA Inspection 893333 — Aeterna Zentaris Gmbh

Aeterna Zentaris Gmbh — FEI 3006524368

The FDA completed an inspection of Aeterna Zentaris Gmbh on Aug 26, 2014 in Frankfurt am Main. 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
Aug 26, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Frankfurt am Main (Germany)

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