FDA Inspection 927930 — CUP Laboratorien Dr. Freitag GmbH

CUP Laboratorien Dr. Freitag GmbH — FEI 3010163518

The FDA completed an inspection of CUP Laboratorien Dr. Freitag GmbH on May 8, 2015 in Radeberg. 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
May 8, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Radeberg (Germany)

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