FDA Inspection 1080035 — Curia Italy S.R.L

Curia Italy S.R.L — FEI 3004999657

The FDA completed an inspection of Curia Italy S.R.L on Mar 22, 2018 in Rozzano. 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
Mar 22, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rozzano (Italy)

Additional details

Mutual Recognition Agreement (MRA)

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