FDA Inspection 1237155 — Bernardy

Bernardy — FEI 3009180055

The FDA completed an inspection of Bernardy on Apr 26, 2024 in Thenioux. 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
Apr 26, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Thenioux (France)