FDA Inspection 1284260 — HPF SRL

HPF SRL — FEI 3009546990

The FDA completed an inspection of HPF SRL on September 11, 2025 in Forgaria Nel Friuli. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 11, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Forgaria Nel Friuli (Italy)

Citations

IDCFRDescription
315921 CFR 820.184DHR content
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation