FDA Inspection 995893 — Socoplan

Socoplan — FEI 3009556071

The FDA completed an inspection of Socoplan on Jul 22, 2016 in Thouars Cedex. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 22, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Thouars Cedex (France)