FDA Inspection 1156199 — Pekana Naturheilmittel GmbH

Pekana Naturheilmittel GmbH — FEI 3002037061

The FDA completed an inspection of Pekana Naturheilmittel GmbH on July 22, 2021 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
July 22, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kislegg (Germany)

Additional Details

Mutual Recognition Agreement (MRA)