FDA Inspection 1062225 — Herbamed AG

Herbamed AG — FEI 1000343707

The FDA completed an inspection of Herbamed AG on July 13, 2018 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
July 13, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Buhler (Switzerland)