FDA Inspection 907150 — IMS GIOTTO S.P.A.

IMS GIOTTO S.P.A. — FEI 3002807317

The FDA completed an inspection of IMS GIOTTO S.P.A. on Dec 4, 2014 in Sasso Marconi. 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
Dec 4, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Sasso Marconi (Italy)

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