FDA Inspection 1117145 — Interquim S.A.

Interquim S.A. — FEI 3002807304

The FDA completed an inspection of Interquim S.A. on Dec 20, 2018 in Sant Cugat Del Valles. 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 20, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sant Cugat Del Valles (Spain)

Additional Details

Mutual Recognition Agreement (MRA)

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