FDA Inspection 863242 — 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 December 5, 2013 in Ravensburg. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 5, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ravensburg (Germany)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures