FDA Inspection 1156199 — Pekana Naturheilmittel GmbH

Pekana Naturheilmittel GmbH — FEI 3002037061

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

Additional Details

Mutual Recognition Agreement (MRA)

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