FDA Inspection 1312428 — Interquim S.A.

Interquim S.A. — FEI 3002807304

The FDA completed an inspection of Interquim S.A. on Sep 6, 2024 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
Sep 6, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sant Cugat Del Valles (Spain)

Additional Details

Mutual Recognition Agreement (MRA)

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