FDA Inspection 857139 — Herbamed AG

Herbamed AG — FEI 1000343707

The FDA completed an inspection of Herbamed AG on December 6, 2013 in Buhler. 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
December 6, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Buhler (Switzerland)