FDA Inspection 1143607 — IDT Biologika GmbH

IDT Biologika GmbH — FEI 3005001757

The FDA completed an inspection of IDT Biologika GmbH on Sep 10, 2020 in Dessau-Rosslau. 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
Sep 10, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dessau-Rosslau (Germany)

Additional details

Mutual Recognition Agreement (MRA)

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