FDA Inspection 1234785 — Videomed SRL

Videomed SRL — FEI 3019252669

The FDA completed an inspection of Videomed SRL on Mar 21, 2024 in Pordenone. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 21, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Pordenone (Italy)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
315921 CFR 820.184DHR content