FDA Inspection 782629 — Vetter Pharma Fertigung GmbH & Co. KG

Vetter Pharma Fertigung GmbH & Co. KG — FEI 3002270322

The FDA completed an inspection of Vetter Pharma Fertigung GmbH & Co. KG on April 17, 2012 in Ravensburg. 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
April 17, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ravensburg (Germany)