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 or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 6, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kislegg (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.