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 December 4, 2014 in Sasso Marconi. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 4, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Sasso Marconi (Italy)