FDA Inspection 788970 — Nuvisan GmbH

Nuvisan GmbH — FEI 3002809479

The FDA completed an inspection of Nuvisan GmbH on May 16, 2012 in Neu-Ulm. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 16, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Neu-Ulm (Germany)