FDA Inspection 945426 — Ursapharm Arzneimittel GmbH

Ursapharm Arzneimittel GmbH — FEI 3004978466

The FDA completed an inspection of Ursapharm Arzneimittel GmbH on Sep 25, 2015 in Saarbrucken. 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, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saarbrucken (Germany)

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