FDA Inspection 1265082 — Friedrich Daniels GMBH

Friedrich Daniels GMBH — FEI 3002806773

The FDA completed an inspection of Friedrich Daniels GMBH on March 26, 2025 in Solingen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 26, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Solingen (Germany)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained