FDA Inspection 981424 — Pekana Naturheilmittel GmbH

Pekana Naturheilmittel GmbH — FEI 3002037061

The FDA completed an inspection of Pekana Naturheilmittel GmbH on May 6, 2016 in Kislegg. 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
May 6, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kislegg (Germany)