FDA Inspection 1312428 — Interquim S.A.
The FDA completed an inspection of Interquim S.A. on September 6, 2024 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 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)