FDA Inspection 1010367 — Roquette Freres

Roquette Freres — FEI 1000114558

The FDA completed an inspection of Roquette Freres on February 10, 2017 in Lestrem. 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
February 10, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lestrem (France)