FDA Inspection 1269800 — Aakamp GmbH

Aakamp GmbH — FEI 3014262024

The FDA completed an inspection of Aakamp GmbH on May 14, 2025 in Breddorf. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 14, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Breddorf (Germany)

Citations

IDCFRDescription
2284321 CFR 111.70(b)Specifications - components
2284721 CFR 111.70(e)Specifications - finished dietary supplement
2288821 CFR 111.210Master manufacturing record - record requirements