FDA Inspection 1276103 — Menadiona S.A.

Menadiona S.A. — FEI 1000242648

The FDA completed an inspection of Menadiona S.A. on Jul 10, 2024 in Palafolls. 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
Jul 10, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Palafolls (Spain)

Additional Details

Mutual Recognition Agreement (MRA)