FDA Inspection 1277384 — Boiron

Boiron — FEI 3004611192

The FDA completed an inspection of Boiron on September 15, 2023 in Messimy. 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 15, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Messimy (France)

Additional Details

Mutual Recognition Agreement (MRA)