FDA Inspection 1200410 — ADRIA SRL

ADRIA SRL — FEI 3014200871

The FDA completed an inspection of ADRIA SRL on Mar 16, 2023 in Poggio Rusco. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 16, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Poggio Rusco (Italy)

Citations

IDCFRDescription
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.