FDA Inspection 933400 — Rentschler Biopharma SE

Rentschler Biopharma SE — FEI 1000291122

The FDA completed an inspection of Rentschler Biopharma SE on June 16, 2015 in Laupheim. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 16, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Laupheim (Germany)