FDA Inspection 1062923 — Sanochemia Pharmazeutika Ag

Sanochemia Pharmazeutika Ag — FEI 3001319566

The FDA completed an inspection of Sanochemia Pharmazeutika Ag on Dec 11, 2017 in Neufeld An Der Leitha. 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
Dec 11, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Neufeld An Der Leitha (Austria)

Additional Details

Mutual Recognition Agreement (MRA)

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