FDA Inspection 1031096 — ITG Int.

ITG Int. — FEI 3005627946

The FDA completed an inspection of ITG Int. on Oct 20, 2017 in Oxford, OH. 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
Oct 20, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Oxford, OH (United States)