FDA Inspection 1101076 — Centrient Pharmaceuticals Spain S.A.

Centrient Pharmaceuticals Spain S.A. — FEI 3003754230

The FDA completed an inspection of Centrient Pharmaceuticals Spain S.A. on May 10, 2019 in Santa Perpetua De Mogoda. 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
May 10, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Santa Perpetua De Mogoda (Spain)

Additional Details

Mutual Recognition Agreement (MRA)