FDA Inspection 744719 — Rentschler Biopharma SE

Rentschler Biopharma SE — FEI 1000291122

The FDA completed an inspection of Rentschler Biopharma SE on Jul 19, 2011 in Laupheim. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 19, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Laupheim (Germany)

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