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FDA Inspection 1014748 — Interquim S.A.

Interquim S.A. — FEI 3002807304

The FDA completed an inspection of Interquim S.A. on June 2, 2017 in Sant Cugat Del Valles. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 2, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sant Cugat Del Valles (Spain)

Facility

Other inspections at this facility

  • 1312428 (VAI Fri Sep 06 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1105907 (VAI Fri Sep 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1117145 (VAI Thu Dec 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 969373 (OAI Fri May 06 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 855632 (VAI Fri Oct 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources