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FDA Inspection 787370 — Interquim S.A.

Interquim S.A. — FEI 3002807304

The FDA completed an inspection of Interquim S.A. on September 9, 2011 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
September 9, 2011
Fiscal Year
2011
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))
  • 1014748 (VAI Fri Jun 02 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 969373 (OAI Fri May 06 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources