FDA Inspection 622471 — Menadiona S.A.

Menadiona S.A. — FEI 1000242648

The FDA completed an inspection of Menadiona S.A. on Oct 1, 2009 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
Oct 1, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Palafolls (Spain)