FDA Inspection 1081751 — Kerr Italia SRL

Kerr Italia SRL — FEI 1000231788

The FDA completed an inspection of Kerr Italia SRL on Feb 6, 2019 in Scafati. 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
Feb 6, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Scafati (Italy)

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