FDA Inspection 1253538 — Socoplan

Socoplan — FEI 3009556071

The FDA completed an inspection of Socoplan on Sep 27, 2024 in Thouars Cedex. 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 27, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Thouars Cedex (France)