FDA Inspection 1116630 — Aea Srl

Aea Srl — FEI 3006571738

The FDA completed an inspection of Aea Srl on Jan 10, 2020 in Maiolati Spontini. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 10, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Maiolati Spontini (Italy)

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